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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
Bed blanket, single-use FDA UDI
Device Name
Blanket Therapeutic Hypo Hyperthermia Pediatric Polyurethane 24 X 30 Inch Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference
HTB030 FDA UDI
Description
Blanket Therapeutic Hypo Hyperthermia Pediatric Polyurethane 24 X 30 Inch Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632112614 FDA UDI
FDA Product Code
ILO FDA UDI
GMDN Term
Bed blanket, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5720 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

No

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: Bed blanket, 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 Bed blanket, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 548656a5-6932-45d5-8e39-6441cdcf7a5d 33 fields · synced May 30, 2026