Curaplex

FDA UDI

Class I (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name: Curaplex FDA UDI
Generic Name: Bed blanket, single-use FDA UDI
Device Name: Curaplex Polyester Gray Blanket 66" x 90", 8/CS FDA UDI
Model / Reference: 3272-53578 FDA UDI
Description: Curaplex Polyester Gray Blanket 66" x 90", 8/CS FDA UDI

Identifiers

Catalog Number: 3272-53578 FDA UDI
Primary DI / UDI-DI: 00810071633300 FDA UDI
FDA Product Code: KME FDA UDI
GMDN Term: Bed blanket, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6060 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Bed blanket, single-use

Curaplex by Bound Tree Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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AllCare — ALLCARE, INC. · Class I
ALLCARE — ALLCARE, INC. · Class I
Bosma Enterprises — Bosma Enterprises · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Bound Tree Medical, Llc

Sources (1)

FDA UDI d7250f17-f6e9-40d9-9a17-4b86d1cb17b3 34 fields · synced May 31, 2026