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Adc®

FDA UDI

Class I (US FDA UDI)

by American Diagnostic Corporation

Identity

Trade Name
ADC® FDA UDI
Generic Name
Intraocular scissors, conventional-hinge, reusable FDA UDI
Device Name
Iris Scissors, Str,4-1/2", Disp pkg FDA UDI
Model / Reference
3424Q FDA UDI
Description
Iris Scissors, Str,4-1/2", Disp pkg FDA UDI

Identifiers

Catalog Number
3424Q FDA UDI
Primary DI / UDI-DI
00634782036294 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Intraocular scissors, conventional-hinge, 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 4.5 Inch FDA UDI

Category: Intraocular scissors, conventional-hinge, reusable

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

Similar devices

Also classified as Intraocular scissors, conventional-hinge, 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 b2c04571-bb6b-4cb6-b5cc-f2f4ebe8f85b 36 fields · synced Jun 8, 2026