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Rumex

FDA UDI

Class I (US FDA UDI)

by Rumex International Co.

Identity

Trade Name
Rumex FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
Tennant Angled Tying Forceps, Extra Delicate Tips, For 9-0 to 11-0 Sutures, Round Handle, Titanium FDA UDI
Model / Reference
4-1851T FDA UDI
Description
Tennant Angled Tying Forceps, Extra Delicate Tips, For 9-0 to 11-0 Sutures, Round Handle, Titanium FDA UDI

Identifiers

Catalog Number
4-1851T FDA UDI
Primary DI / UDI-DI
00840159906279 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

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: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Rumex by Rumex International Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue manipulation 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 159719a2-e8fe-4457-8f80-ed50ac918ce4 34 fields · synced Jun 9, 2026