← Back to catalogue

Vera Fixation Hook For Xen Stent

FDA UDI

Class I (US FDA UDI)

by Katena Products, Inc.

Identity

Trade Name
VERA FIXATION HOOK FOR XEN STENT FDA UDI
Generic Name
Eyeball fixation instrument, reusable FDA UDI
Device Name
VERA FIXATION HOOK FOR XEN STENT FDA UDI
Model / Reference
AE-2588 FDA UDI
Description
VERA FIXATION HOOK FOR XEN STENT FDA UDI

Identifiers

Catalog Number
AE-2588 FDA UDI
Primary DI / UDI-DI
00841668130292 FDA UDI
FDA Product Code
HNQ FDA UDI
GMDN Term
Eyeball fixation instrument, 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: Eyeball fixation instrument, reusable

Vera Fixation Hook For Xen Stent by Katena Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eyeball fixation instrument, 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 4d8f83ac-c332-4d07-a4d2-c6629bf38edf 35 fields · synced Jun 12, 2026