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CSP, Premature Nasal Cannula

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
CSP,Premature Nasal Cannula FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
CSP,Premature Nasal Cannula,High Flow, adapters, Yellow FDA UDI
Model / Reference
0883 FDA UDI
Description
CSP,Premature Nasal Cannula,High Flow, adapters, Yellow FDA UDI

Identifiers

Primary DI / UDI-DI
00709078003813 FDA UDI
FDA Product Code
CAT FDA UDI
GMDN Term
Nasal oxygen cannula, basic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
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

No

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

CSP, Premature Nasal Cannula 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 00fcc1c6-a7e0-4e22-878e-b713d2de4ab8 34 fields · synced Jun 8, 2026