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Medichoice

FDA UDI

Class II (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
Medichoice FDA UDI
Generic Name
Umbilical cord clamp, single-use FDA UDI
Device Name
Clamp White Double grip 8cm HDPE White CA/500 Replaces CLMP101 Not made with Natural Rubber Latex MediChoice FDA UDI
Model / Reference
55751 FDA UDI
Description
Clamp White Double grip 8cm HDPE White CA/500 Replaces CLMP101 Not made with Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632431364 FDA UDI
FDA Product Code
HFW FDA UDI
GMDN Term
Umbilical cord clamp, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 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: Umbilical cord clamp, single-use

Medichoice by Owens & Minor Distribution, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Umbilical cord clamp, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 034a45c4-80e6-49a8-9f04-557de177a933 33 fields · synced May 31, 2026