← Back to catalogue

Circuit Tubing

FDA UDI

Class I (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
Circuit Tubing FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
Performance Tubing 6ft (1.83m), China FDA UDI
Model / Reference
Performance Tubing, 6 ft. (1.83m), White, CN FDA UDI
Description
Performance Tubing 6ft (1.83m), China FDA UDI

Identifiers

Catalog Number
CN1032907 FDA UDI
Primary DI / UDI-DI
00606959050952 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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, single-use

Circuit Tubing by Respironics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ventilator breathing circuit, single-use.

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 d924ccf0-02d9-4176-9418-726692b998fd 36 fields · synced May 30, 2026