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Oph. Retractor

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
Oph. Retractor FDA UDI
Generic Name
Periocular/lacrimal retractor, hand-held, reusable FDA UDI
Device Name
Knapp (Rollet) Retractor, 4 Sharp Prongs FDA UDI
Model / Reference
08-05101 FDA UDI
Description
Knapp (Rollet) Retractor, 4 Sharp Prongs FDA UDI

Identifiers

Catalog Number
08-05101 FDA UDI
Primary DI / UDI-DI
00841668119068 FDA UDI
FDA Product Code
HNI FDA UDI
GMDN Term
Periocular/lacrimal retractor, hand-held, 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

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: Periocular/lacrimal retractor, hand-held, reusable

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

Similar devices

Also classified as Periocular/lacrimal retractor, hand-held, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katena Products, Inc.

Sources (1)

  • FDA UDI 73dea7c1-0d5d-42ae-bc4f-4cb3e8ac50f8 35 fields · synced Jun 12, 2026