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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, scissors-like, single-use FDA UDI
Device Name
ST. STR MOSQUITO HEMOSTAT 3 1/2'(MHB700) FDA UDI
Model / Reference
67325 FDA UDI
Description
ST. STR MOSQUITO HEMOSTAT 3 1/2'(MHB700) FDA UDI

Identifiers

Catalog Number
67325 FDA UDI
Primary DI / UDI-DI
00653160110678 FDA UDI
FDA Product Code
HRQ FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, scissors-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, scissors-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, scissors-like, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3c6656c6-5d0f-414b-869c-f436557ddcf5 35 fields · synced May 31, 2026