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Adc®

FDA UDI

Class I (US FDA UDI)

by American Diagnostic Corporation

Identity

Trade Name
ADC® FDA UDI
Generic Name
Utility forceps, reusable FDA UDI
Device Name
Kelly Forceps, Curved,5-1/2", Silver, Disp pkg FDA UDI
Model / Reference
311Q FDA UDI
Description
Kelly Forceps, Curved,5-1/2", Silver, Disp pkg FDA UDI

Identifiers

Catalog Number
311Q FDA UDI
Primary DI / UDI-DI
00634782020767 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Utility forceps, reusable 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Dimensions & Sizes

Size
Length — 5.5 Inch FDA UDI

Category: Utility forceps, reusable

Adc® by American Diagnostic Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Utility forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
American Diagnostic Corporation

Sources (1)

  • FDA UDI 09b256d1-537e-4d50-87da-3bfc681c4e70 36 fields · synced Jun 8, 2026