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OTS PG&E Field Kit

FDA UDI

Class N (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name
OTS PG&E Field Kit FDA UDI
Generic Name
Endothermic cold therapy pack FDA UDI
Device Name
OTS PG&E Field Kit FDA UDI
Model / Reference
K610-703 FDA UDI
Description
OTS PG&E Field Kit FDA UDI

Identifiers

Catalog Number
K610-703 FDA UDI
Primary DI / UDI-DI
00766588107035 FDA UDI
FDA Product Code
LRR FDA UDI
EFQ FDA UDI
IMD FDA UDI
CBP FDA UDI
GMDN Term
Endothermic cold therapy pack FDA UDI

Classification

Device Class
N FDA UDI
Regulation Number
890.5710 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

OTS PG&E Field Kit 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 9a480452-c0aa-4c40-8d53-ced06d67cdd5 35 fields · synced Jun 8, 2026