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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
Surgical soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI
Device Name
Debakey Tangential 10 1/2" Length FDA UDI
Model / Reference
Debakey Forceps FDA UDI
Description
Debakey Tangential 10 1/2" Length FDA UDI

Identifiers

Catalog Number
505245 FDA UDI
Primary DI / UDI-DI
B97450524507 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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 — 10.5 Inch FDA UDI

Category: Surgical soft-tissue manipulation forceps, tweezers-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 Surgical soft-tissue manipulation forceps, tweezers-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 85c3810c-01be-4702-ae76-3e3cb8d532e8 35 fields · synced Jun 8, 2026