← Back to catalogue

Coldpack 7" X 11" (if Not Avail Use 32187)

FDA UDI

Class I (US FDA UDI)

by AliMed, LLC

Identity

Trade Name
COLDPACK 7" X 11" (IF NOT AVAIL USE 32187) FDA UDI
Generic Name
Hot/cold therapy pack, reusable FDA UDI
Model / Reference
32704 FDA UDI

Identifiers

Catalog Number
2970000981 FDA UDI
Primary DI / UDI-DI
00733657225075 FDA UDI
FDA Product Code
IME FDA UDI
GMDN Term
Hot/cold therapy pack, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5700 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hot/cold therapy pack, reusable

Coldpack 7" X 11" (if Not Avail Use 32187) by AliMed, 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
AliMed, LLC

Sources (1)

  • FDA UDI fc97ecaf-45cc-444d-b26c-7ca2f583a1ab 34 fields · synced Jun 9, 2026