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16PW - Class A Burn Relief

FDA UDI

Class I (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name
16PW - Class A Burn Relief FDA UDI
Generic Name
Non-rebreathing valve, single-use FDA UDI
Device Name
16PW - Class A Burn Relief FDA UDI
Model / Reference
K616-062 FDA UDI
Description
16PW - Class A Burn Relief FDA UDI

Identifiers

Catalog Number
K616-062 FDA UDI
Primary DI / UDI-DI
00766588160627 FDA UDI
FDA Product Code
IMD FDA UDI
LRR FDA UDI
HMP FDA UDI
KGX FDA UDI
EFQ FDA UDI
CBP FDA UDI
GMDN Term
Non-rebreathing valve, single-use FDA UDI

Classification

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

16PW - Class A Burn Relief by Certified Safety Manufacturing, Inc. — Class I — 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 0db69c2b-0d14-4919-958d-fea19312ef5a 35 fields · synced Jun 8, 2026