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Curaplex

FDA UDI

Class I (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Hot/cold therapy pack, reusable FDA UDI
Device Name
Curaplex Hot Pack, Large FDA UDI
Model / Reference
1431-16012 FDA UDI
Description
Curaplex Hot Pack, Large FDA UDI

Identifiers

Catalog Number
1431-16012 FDA UDI
Primary DI / UDI-DI
00817617025193 FDA UDI
FDA Product Code
IDM FDA UDI
GMDN Term
Hot/cold therapy pack, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 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

Yes

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

Yes

FDA UDI

Category: Hot/cold therapy pack, reusable

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

Similar devices

Also classified as Hot/cold therapy pack, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8edec9ca-55e3-4dda-beb2-5c7a2be16b51 34 fields · synced May 30, 2026