← Back to catalogue

Nishi Schlemm's Canal Scissors

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
NISHI SCHLEMM'S CANAL SCISSORS FDA UDI
Generic Name
Corneal scissors, reusable FDA UDI
Device Name
NISHI SCHLEMM'S CANAL SCISSORS FDA UDI
Model / Reference
AE-5669 FDA UDI
Description
NISHI SCHLEMM'S CANAL SCISSORS FDA UDI

Identifiers

Catalog Number
AE-5669 FDA UDI
Primary DI / UDI-DI
00841668137376 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Corneal scissors, 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: Corneal scissors, reusable

Nishi Schlemm's Canal Scissors by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneal scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a481b024-479f-40fc-ab3d-476b68ad7561 35 fields · synced Jun 12, 2026