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Forceps

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
FORCEPS FDA UDI
Generic Name
Dressing/utility forceps, scissors-like, single-use FDA UDI
Device Name
SPONGE FORCEPS 7" FDA UDI
Model / Reference
SPONGE FORCEPS FDA UDI
Description
SPONGE FORCEPS 7" FDA UDI

Identifiers

Catalog Number
EA600 FDA UDI
Primary DI / UDI-DI
B974EA6000 FDA UDI
FDA Product Code
GEN 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

No

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI

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

Forceps by Dr.frigz International(pvt)ltd, — 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
Dr.frigz International(pvt)ltd,

Sources (1)

  • FDA UDI 1410e079-1af9-44f7-9c98-f338ce822fa5 35 fields · synced May 31, 2026