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Anodyne Surgical

FDA UDI

Class I (US FDA UDI)

by Psi/Eye-Ko, Inc.

Identity

Trade Name
Anodyne Surgical FDA UDI
Generic Name
Intraocular scissors probe-tip, reusable FDA UDI
Device Name
Westcott Stitch Scissors, Curved Very Sharp Tips 22mm, Serrated handle, SS FDA UDI
Model / Reference
CT2001 FDA UDI
Description
Westcott Stitch Scissors, Curved Very Sharp Tips 22mm, Serrated handle, SS FDA UDI

Identifiers

Primary DI / UDI-DI
00840516130927 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Intraocular scissors probe-tip, 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intraocular scissors probe-tip, reusable

Anodyne Surgical by Psi/Eye-Ko, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraocular scissors probe-tip, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Psi/Eye-Ko, Inc.

Sources (1)

  • FDA UDI 17eb423f-8924-4400-82de-135fea0d1811 34 fields · synced May 30, 2026