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Oph.Forceps

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Oph.Forceps FDA UDI
Generic Name
Dressing/utility forceps, tweezers-like, reusable FDA UDI
Device Name
Jeweler Forceps, #4, Straight FDA UDI
Model / Reference
08-01607 FDA UDI
Description
Jeweler Forceps, #4, Straight FDA UDI

Identifiers

Catalog Number
08-01607 FDA UDI
Primary DI / UDI-DI
00841668118054 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Dressing/utility forceps, tweezers-like, 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

Yes

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, tweezers-like, reusable

Oph.Forceps by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dressing/utility forceps, tweezers-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1385b5d7-38a2-4c75-85c0-d1dc59e1cc67 35 fields · synced Jun 12, 2026