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Rumex

FDA UDI

Class I (US FDA UDI)

by Rumex International Co.

Identity

Trade Name
Rumex FDA UDI
Generic Name
Intraocular scissors, probe-like, reusable FDA UDI
Device Name
Barraquer Iris Scissors, Blunt Tips, 8.00 mm From Bend To Tip, Flat Serrated Squeeze Action Handle With Polished Finish, Length 54 mm (2.10 inches), Stainless Steel FDA UDI
Model / Reference
11-1223 FDA UDI
Description
Barraquer Iris Scissors, Blunt Tips, 8.00 mm From Bend To Tip, Flat Serrated Squeeze Action Handle With Polished Finish, Length 54 mm (2.10 inches), Stainless Steel FDA UDI

Identifiers

Catalog Number
11-1223 FDA UDI
Primary DI / UDI-DI
00840159905043 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular scissors, probe-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: Intraocular scissors, probe-like, reusable

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

Similar devices

Also classified as Intraocular scissors, probe-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 04bc3415-e1ff-450f-b87e-502bf71472da 34 fields · synced Jun 9, 2026