← Back to catalogue

Medi-First Flexible Patch HW

FDA UDI

Class I (US FDA UDI)

by Medique Products

Identity

Trade Name
Medi-First Flexible Patch HW FDA UDI
Generic Name
Skin-cover adhesive strip, non-antimicrobial FDA UDI
Device Name
Flexible patch of fabric material coated on one side with a pressure-sensitive adhesive and with an absorbent pad intended to cover a superficial wound. FDA UDI
Model / Reference
61973 FDA UDI
Description
Flexible patch of fabric material coated on one side with a pressure-sensitive adhesive and with an absorbent pad intended to cover a superficial wound. FDA UDI

Identifiers

Catalog Number
61973 FDA UDI
Primary DI / UDI-DI
00347682619732 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Skin-cover adhesive strip, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 FDA UDI
Commercial Distribution
Not 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Medi-First Flexible Patch HW by Medique Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Medique Products

Sources (1)

  • FDA UDI 09c81261-4aa4-445e-a13d-99aff99abdbd 35 fields · synced Jun 8, 2026