← Back to catalogue

O2 Enrichment Attachment

FDA UDI

Class I (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
O2 Enrichment Attachment FDA UDI
Generic Name
Ventilator breathing circuit, reusable FDA UDI
Device Name
O2 Enrichment Attachment, box of 10 FDA UDI
Model / Reference
O2 Enrichment Attachment FDA UDI
Description
O2 Enrichment Attachment, box of 10 FDA UDI

Identifiers

Catalog Number
312010 FDA UDI
Primary DI / UDI-DI
00606959002593 FDA UDI
FDA Product Code
CAI FDA UDI
GMDN Term
Ventilator breathing circuit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Category: Ventilator breathing circuit, reusable

O2 Enrichment Attachment by Respironics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI 9cc161ea-766a-49bf-9e08-21700ac8fe27 36 fields · synced Jun 8, 2026