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25ga iQ™ Super Grip Forceps

FDA UDI

Class I (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
25ga iQ™ Super Grip Forceps FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, probe-like, reusable FDA UDI
Device Name
25ga iQ™ Super Grip Forceps FDA UDI
Model / Reference
RVF4034-25 FDA UDI
Description
25ga iQ™ Super Grip Forceps FDA UDI

Identifiers

Primary DI / UDI-DI
00840096210149 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, probe-like, 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

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

Category: Ophthalmic soft-tissue manipulation forceps, probe-like, reusable

25ga iQ™ Super Grip Forceps by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue manipulation forceps, probe-like, reusable.

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 6246582b-87bb-4553-80c8-7261300d8577 33 fields · synced Jun 8, 2026