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Centurion

FDA UDI

Class I (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Centurion FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI
Device Name
STERILE CURV CRILE FORCEP (CF81810) FDA UDI
Model / Reference
66395 FDA UDI
Description
STERILE CURV CRILE FORCEP (CF81810) FDA UDI

Identifiers

Catalog Number
66395 FDA UDI
Primary DI / UDI-DI
00653160044034 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical soft-tissue manipulation forceps, tweezers-like, single-use

Centurion by Centurion Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, tweezers-like, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d6860355-d13f-4f0b-b052-e16da180f841 35 fields · synced Jun 8, 2026