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Titanium Kuglen Iris Hook and Lens Manipulator, Angled

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
Titanium Kuglen Iris Hook and Lens Manipulator, Angled FDA UDI
Generic Name
Ophthalmic surgical probe, reusable FDA UDI
Model / Reference
2000A FDA UDI

Identifiers

Primary DI / UDI-DI
00817489029176 FDA UDI
FDA Product Code
HNQ FDA UDI
GMDN Term
Ophthalmic surgical probe, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Titanium Kuglen Iris Hook and Lens Manipulator, Angled by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katalyst Surgical, Llc

Sources (1)

  • FDA UDI 5496b594-f23c-47f4-87c1-21490d766d90 33 fields · synced May 29, 2026