3M™ ACE™ Brand

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name: 3M™ ACE™ Brand FDA UDI
Generic Name: Hot/cold therapy pack, reusable FDA UDI
Device Name: ACE™ Brand Instant Cold Compress Twin Pack 207514 FDA UDI
Model / Reference: 207514 FDA UDI
Description: ACE™ Brand Instant Cold Compress Twin Pack 207514 FDA UDI

Identifiers

Catalog Number: 207514 FDA UDI
Primary DI / UDI-DI: 30051131198426 FDA UDI
FDA Product Code: IMD FDA UDI
GMDN Term: Hot/cold therapy pack, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.5710 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Hot/cold therapy pack, reusable

3M™ ACE™ Brand by 3m Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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HOT/COLD THERAPEUTIC PACK FOR KNEE — Wuhan Pakcare Bio‐technology Co.,Ltd. · Class I
hot cold pack — Anhui Kamt Ice Pack Co.,Ltd. · Class I
HotCold Pack reusable — Bevaplast B.V. · Class I
reusable cold hot gel pack for Ankle — Wuhan Pakcare Bio‐technology Co.,Ltd. · 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: 3m Company

Sources (1)

FDA UDI 17c3cace-231a-4e3d-be42-7a9ba3e12a18 35 fields · synced Jun 8, 2026