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Dermapac, Inc.

FDA UDI

Class I (US FDA UDI)

by Dermapac Inc.

Identity

Trade Name
Dermapac, Inc. FDA UDI
Generic Name
Dressing/utility forceps, scissors-like, single-use FDA UDI
Device Name
Sponge Forcep - 7" FDA UDI
Model / Reference
9960 FDA UDI
Description
Sponge Forcep - 7" FDA UDI

Identifiers

Primary DI / UDI-DI
10810102271560 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Dressing/utility forceps, scissors-like, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dressing/utility forceps, scissors-like, single-use

Dermapac, Inc. by Dermapac Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dressing/utility forceps, scissors-like, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dermapac Inc.

Sources (1)

  • FDA UDI 3a8c676f-2fde-4a60-9ce3-9714e2dce7b6 34 fields · synced Jun 8, 2026