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Mynx Control

FDA UDI

Class III (US FDA UDI)

by Accessclosure, Inc.

Identity

Trade Name
MYNX CONTROL FDA UDI
Generic Name
Wound hydrogel dressing, non-antimicrobial FDA UDI
Device Name
Mynx Control VCD 6F 7F FDA UDI
Model / Reference
MX6760 FDA UDI
Description
Mynx Control VCD 6F 7F FDA UDI

Identifiers

Catalog Number
MX6760 FDA UDI
Primary DI / UDI-DI
10862028000434 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Wound hydrogel dressing, non-antimicrobial

Mynx Control 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Accessclosure, Inc.

Sources (1)

  • FDA UDI e7d0bf8c-4932-4389-94f6-c07d617a87eb 36 fields · synced Jun 8, 2026