← Back to catalogue

Gas Sampling Line

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Gas Sampling Line FDA UDI
Generic Name
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
Device Name
Gas Sampling Line 10' CoEx PE/PVC, .047" ID x .108" OD, M/M Luers FDA UDI
Model / Reference
0516 FDA UDI
Description
Gas Sampling Line 10' CoEx PE/PVC, .047" ID x .108" OD, M/M Luers FDA UDI

Identifiers

Primary DI / UDI-DI
00709078007934 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Gas-sampling/monitoring respiratory tubing, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5975 FDA UDI
Commercial Distribution
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

Category: Gas-sampling/monitoring respiratory tubing, single-use

Gas Sampling Line by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, 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
Westmed, Inc.

Sources (1)

  • FDA UDI 49c6c7e4-2d1a-4c27-9eed-877d436e0699 33 fields · synced May 31, 2026