← Back to catalogue

pince super grip 27G

FDA UDI

Class I (US FDA UDI)

by Fci S A S Fci 20 22

Identity

Trade Name
pince super grip 27G FDA UDI
Generic Name
Ophthalmic soft-tissue manipulation forceps, probe-like, single-use FDA UDI
Device Name
pince super grip 27G FDA UDI
Model / Reference
S9.6018.27 FDA UDI
Description
pince super grip 27G FDA UDI

Identifiers

Primary DI / UDI-DI
13700773707529 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 27G 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Fci S A S Fci 20 22

Sources (1)

  • FDA UDI e12a5384-dd12-4434-9423-f2fdb07477c4 33 fields · synced Jun 1, 2026