ACE CANNULA 21G 27G 40 mm/50

ACE CANNULA 21G 27G 40 mm/50

ACE MEDICAL

Medical device – blunt microcannula for dermal filler injection
  • Described in international aesthetic congress materials as ACE cannulas with various certificates including CE mark for medical devices used in cosmetic surgery and procedures.
  • Marketed in the European Union as a medical device for filler injection by distributors such as France Health, indicating conformity to applicable European medical device regulations for sterile disposable cannulas.
  • Manufacturer ACE MEDICAL IND, CO., LTD. presents ACE cannulas as certified high Quality blunt tip flexible cannulas for filler injection, fat transfer and fat grafting, with scale mark and dot indicator for precise insertion.
  • ACE cannula products are listed by medical device distributors in multiple regions (including the EU and USA) as sterile single Use medical devices for dermal filler and injectable procedures; detailed classification (e.g. device class and notified body number) is not publicly listed in the consulted sources.
Sterile single-use flexible blunt-tip microcannula 27G x 40 mm (box of 50)

Description

ACE CANNULA 27G-40 mm/50 is a sterile, single-use blunt-tip flexible microcannula manufactured by ACE MEDICAL IND, CO., LTD. (Korea) for injection of dermal fillers and other injectable materials in aesthetic medicine. Marketed as ACE MEDICAL Micro-Cannulas, it is described as a medical device for filler injection with a smooth and clean surface finish produced by electro-chemical machining of the outlet hole, a centimeter scale printed along the shaft for precise depth control, and a dot locator on the hub to indicate the direction of the side opening. The cannula is supplied in a box of 50 units and is part of a gauge/length range that includes 18G, 19G, 21G, 22G, 23G, 24G, 25G, 27G and 30G sizes, all made in Korea for professional medical use.

Bnefits

  • Blunt-tip flexible microcannula designed to reduce tissue trauma compared with sharp hypodermic needles during filler injection procedures.
  • Medical device specifically intended for filler injection and other aesthetic procedures such as fat transfer or fat grafting, according to manufacturer and congress profiles.
  • Smooth and clean surface finishing, including a hole produced by electro-chemical machining at the distal end, described by the manufacturer as providing a smoother surface for injection.
  • Centimeter scale printed on the cannula shaft to help practitioners perform precise, controlled-depth injections.
  • Dot locator printed on the cannula base (hub) so the practitioner can identify the direction of the side opening during injection.
  • Flexible cannula design described by the manufacturer as offering flexibility suitable for various procedures in aesthetic medicine.
  • Supplied sterile and ready for single use in sealed packaging, with 50 cannulas per box for professional clinical settings.
  • Gauge and length combination of 27G x 40 mm, a commonly used configuration for precise filler placement in superficial and mid-depth facial planes.
  • Part of the ACE cannula range that the manufacturer states has obtained various certificates including CE, and is widely used in cosmetic surgery and aesthetic procedure markets.

Indications

  • Use as a blunt-tip flexible microcannula for injection of dermal fillers by trained healthcare professionals in aesthetic medicine.
  • Use in aesthetic procedures such as facial filler injection, fat transfer and fat grafting as described in manufacturer and congress materials for ACE cannulas.
  • Medical device for medical use in procedures where a blunt microcannula is preferred over a sharp needle to facilitate tunnelling and product deposition in soft tissue.

Composition

  • Blunt-tip flexible microcannula with a side-opening hole at the distal end; the hole is described by the manufacturer as being produced by electro-chemical machining to achieve a smooth surface.
  • Cannula shaft marked with a centimeter scale to assist with precise insertion depth during injections.
  • Hub with a printed dot locator indicating the direction of the side opening for accurate orientation during filler delivery.
  • Gauge and length for this specific product: 27G x 40 mm, as listed in ACE cannula gauge/length tables and distributor pages.
  • Supplied as sterile single-use microcannulas for medical use, 50 pieces per box, made in Korea by ACE MEDICAL IND, CO., LTD.
  • Base materials (e.g. specific metals, polymers or coatings) are not publicly listed in the accessible manufacturer or distributor documentation.

Formulation

  • Medical device configuration: sterile, single-use flexible blunt-tip microcannula for soft tissue injection.
  • Design features include a closed blunt tip with a side-opening outlet, a smooth internal and external surface, centimeter scale markings and a hub dot locator.
  • Gauge/length specification: 27G x 40 mm; ACE cannula range also includes 18GX50mm, 18GX70mm, 19GX50mm, 19GX70mm, 21GX50mm, 21GX70mm, 22GX50mm, 22GX70mm, 23GX50mm, 23GX70mm, 24GX40mm, 24GX50mm, 25GX40mm, 25GX50mm, 27GX40mm, 27GX50mm and 30GX25mm, all supplied as 50 pieces per box.
  • Manufactured in Korea by ACE MEDICAL IND, CO., LTD. under the ACE cannula product line, described as having certified high quality and flexibility suitable for various aesthetic procedures.

Packaging

  • Box containing 50 sterile ACE microcannulas (27G x 40 mm), as stated by manufacturer and distributors.
  • Each cannula supplied individually sterile-packed for single use (exact primary packaging materials are not publicly listed).
  • Outer packaging identified and marketed as ACE CANNULA 27G-40 mm/50, with branding ACE MEDICAL and made in Korea; detailed artwork and packaging materials are not publicly listed.

Usage

  • Not publicly listed – healthcare professionals are instructed to follow the instructions for use (IFU) supplied with the ACE Cannula product and to use it only in accordance with applicable training, local regulations and the filler manufacturer’s guidelines.

Contraindications

  • Not publicly listed
  • Clinicians must refer to the official instructions for use (IFU) provided with the ACE Cannula product and to the contraindications of the injectable product (e.g. dermal filler) being administered.

Adverse Effects

  • Not publicly listed
  • Potential risks and adverse events associated with the use of blunt microcannulas for filler injection are typically described in the device IFU and in the product information for the injectable filler rather than in publicly accessible marketing descriptions.

Storage Conditions

  • Not publicly listed
  • As a sterile medical device, storage conditions and expiry information are expected to be specified on the product labelling and packaging (e.g. protection from excessive heat, moisture and damage to sterile packaging), but detailed conditions are not provided in the accessible online product descriptions.

Duration

Not applicable \u2013 this is a sterile single-use medical device (microcannula) used to perform injection procedures; it does not define a pharmacological treatment course or duration.

Onset

Not applicable \u2013 medical device microcannula used to deliver injectable products; onset of effect depends on the injected filler or substance, not on the cannula itself.

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