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O2 Kit: Peoples Medical

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
O2 Kit: Peoples Medical FDA UDI
Generic Name
Oxygen administration tubing FDA UDI
Device Name
O2 Kit Peoples Medical: 6-0556, 6-0194, 4-barbed Con, 3-0052, 1N FDA UDI
Model / Reference
0876 FDA UDI
Description
O2 Kit Peoples Medical: 6-0556, 6-0194, 4-barbed Con, 3-0052, 1N FDA UDI

Identifiers

Primary DI / UDI-DI
00709078002663 FDA UDI
FDA Product Code
OGL FDA UDI
BYX FDA UDI
CAT FDA UDI
GMDN Term
Oxygen administration tubing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5655 FDA UDI
868.5860 FDA UDI
868.5340 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

O2 Kit: Peoples Medical by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 27dee3f1-ce5d-4554-b64e-cdefa9b9c3f6 34 fields · synced May 31, 2026