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Composite Respiratory Kit

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Composite Respiratory Kit FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
1 - Packaged 50' O2 Tubing (0052), 6 - Packaged Soft Cannula with 7' Tubing (0556), 1 - Barbed Connector (40076), 1 - Cylinder Wrench (20014), 1 - Key Chain (90027), 1 - No Smoking Sign (70816). FDA UDI
Model / Reference
0767 FDA UDI
Description
1 - Packaged 50' O2 Tubing (0052), 6 - Packaged Soft Cannula with 7' Tubing (0556), 1 - Barbed Connector (40076), 1 - Cylinder Wrench (20014), 1 - Key Chain (90027), 1 - No Smoking Sign (70816). FDA UDI

Identifiers

Primary DI / UDI-DI
00709078003615 FDA UDI
FDA Product Code
BYX FDA UDI
OGL FDA UDI
CAT FDA UDI
GMDN Term
Nasal oxygen cannula, basic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 FDA UDI
868.5655 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

Composite Respiratory Kit by Westmed, Inc. — Class I — 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 2d7436aa-9a16-4ff6-845f-7cb7296fdb2a 34 fields · synced Jun 6, 2026