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75V - UP Facilities

FDA UDI

Class N (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name
75V - UP Facilities FDA UDI
Generic Name
Non-rebreathing valve, single-use FDA UDI
Device Name
75V - UP Facilities FDA UDI
Model / Reference
K612-166 FDA UDI
Description
75V - UP Facilities FDA UDI

Identifiers

Catalog Number
K612-166 FDA UDI
Primary DI / UDI-DI
00766588121666 FDA UDI
FDA Product Code
LRR FDA UDI
EFQ FDA UDI
KGX FDA UDI
IMD FDA UDI
CBP FDA UDI
GMDN Term
Non-rebreathing valve, single-use FDA UDI

Classification

Device Class
N FDA UDI
Regulation Number
880.5240 FDA UDI
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 padDressing-fixation skin adhesive tape, non-silicone

75V - UP Facilities 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 6ea8af76-e71a-4c54-822e-aaebfbf21e80 35 fields · synced Jun 8, 2026