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Centurion

FDA UDI

Class I (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Centurion FDA UDI
Generic Name
Umbilical cord clamp/cutter FDA UDI
Device Name
UMBILICAL CORD CLAMP CLIPPER FDA UDI
Model / Reference
CTR300 FDA UDI
Description
UMBILICAL CORD CLAMP CLIPPER FDA UDI

Identifiers

Catalog Number
CTR300 FDA UDI
Primary DI / UDI-DI
00653160120561 FDA UDI
FDA Product Code
KOH FDA UDI
GMDN Term
Umbilical cord clamp/cutter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4520 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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: Umbilical cord clamp/cutter

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

Similar devices

Also classified as Umbilical cord clamp/cutter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 36a36f9f-8084-42c8-bb58-ab26ef1a34c0 35 fields · synced Jun 8, 2026