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FAC-4 - Hensel Phelps

FDA UDI

Class N (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name
FAC-4 - Hensel Phelps FDA UDI
Generic Name
Endothermic cold therapy pack FDA UDI
Device Name
FAC-4 - Hensel Phelps FDA UDI
Model / Reference
K609-079 FDA UDI
Description
FAC-4 - Hensel Phelps FDA UDI

Identifiers

Catalog Number
K609-079 FDA UDI
Primary DI / UDI-DI
00766588090795 FDA UDI
FDA Product Code
LRR FDA UDI
EFQ FDA UDI
KGX FDA UDI
HMP FDA UDI
CBP FDA UDI
IMD FDA UDI
GMDN Term
Endothermic cold therapy pack FDA UDI

Classification

Device Class
N FDA UDI
Regulation Number
880.5240 FDA UDI
878.4440 FDA UDI
868.5870 FDA UDI
890.5710 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: First aid kit, medicatedAdhesive bandageNon-woven gauze padWound-nonadherent dressing, absorbent, non-antimicrobial

FAC-4 - Hensel Phelps by Certified Safety Manufacturing, Inc. — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endothermic cold therapy pack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1b6ff099-9ccf-41c3-b991-d8c2913d684e 35 fields · synced Jun 8, 2026