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pince super grip 23G

FDA UDI

Class I (US FDA UDI)

by Fci S A S Fci 20 22

Identity

Trade Name
pince super grip 23G FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, probe-like, single-use FDA UDI
Device Name
pince super grip 23G FDA UDI
Model / Reference
S9.6018.23 FDA UDI
Description
pince super grip 23G FDA UDI

Identifiers

Primary DI / UDI-DI
13700773707505 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue manipulation forceps, probe-like, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic soft-tissue manipulation forceps, probe-like, single-use

pince super grip 23G by Fci S A S Fci 20 22 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fci S A S Fci 20 22

Sources (1)

  • FDA UDI 040605a8-2c19-44d3-8476-db4376793c22 33 fields · synced Jun 8, 2026