Mynx Ace Vascular Closure Device (6F/7F)

FDA UDI

Class III (US FDA UDI)

by Accessclosure, Inc.

Identity

Trade Name: Mynx Ace Vascular Closure Device (6F/7F) FDA UDI
Generic Name: Wound hydrogel dressing, non-antimicrobial FDA UDI
Device Name: Mynx Ace Vascular Closure Device (6F/7F) FDA UDI
Model / Reference: MX6740 FDA UDI
Description: Mynx Ace Vascular Closure Device (6F/7F) FDA UDI

Identifiers

Catalog Number: MX6740 FDA UDI
Primary DI / UDI-DI: M465MX67400 FDA UDI
PMA Number: P040044 FDA UDI
FDA Product Code: MGB FDA UDI
GMDN Term: Wound hydrogel dressing, non-antimicrobial FDA UDI

Classification

Device Class: Class III FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 6 French FDA UDI

Category: Wound hydrogel dressing, non-antimicrobial

Mynx Ace Vascular Closure Device (6F/7F) by Accessclosure, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound hydrogel dressing, non-antimicrobial.

Orasoothe Oral Coating Rinse 4oz – Hygiene — SEPTODONT SAS SPECIALITES SEPTODONT · Class I
Microcyn Skin & Wound HydroGel — Sonoma Pharmaceuticals, Inc. · U
HydroTac transparent 10x10cm steril P10 — Paul Hartmann Corp. · Class I
Hyalo4 Care Clear Hydrogel, 100g — Fidia Farmaceutici · U
CareOne — Ahold U.S.A., Inc. · Class I
NAR — NORTH AMERICAN RESCUE, LLC. · Class I
Simpurity — SAFE N SIMPLE LLC · Class I
Halo — Medical Devices Inc. · Class I

Cleared under the same submission

P040044 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Accessclosure, Inc.

Sources (1)

FDA UDI bfbb464e-d81a-4103-a6e7-053ddad57f08 38 fields · synced May 31, 2026