Rumex

FDA UDI

Class I (US FDA UDI)

by Rumex International Co.

Identity

Trade Name: Rumex FDA UDI
Generic Name: Intraocular retractor, reusable FDA UDI
Device Name: Knapp Lacrimal Sac Retractor, Sharp 4 x 8 mm Four Prongs Tip, Length 140 mm, Round Serrated Titanium Handle FDA UDI
Model / Reference: 10-114 FDA UDI
Description: Knapp Lacrimal Sac Retractor, Sharp 4 x 8 mm Four Prongs Tip, Length 140 mm, Round Serrated Titanium Handle FDA UDI

Identifiers

Catalog Number: 10-114 FDA UDI
Primary DI / UDI-DI: 00840159909164 FDA UDI
FDA Product Code: HNI FDA UDI
GMDN Term: Intraocular retractor, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Intraocular retractor, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Rumex International Co.

Sources (1)

FDA UDI 88c6a0de-11f8-4d19-b283-ead2f1e9da02 34 fields · synced Jun 9, 2026