← Back to catalogue

Gas Collecting Vessel

FDA UDI

Class I (US FDA UDI)

by Hangzhou A-Tek Medical & Textiles Co., Ltd.

Identity

Trade Name
GAS COLLECTING VESSEL FDA UDI
Generic Name
Exhaled-gas sample collector, non-electronic FDA UDI
Device Name
GAS COLLECTING VESSEL, COLLECT AND STORE GAS SAMPLES OR LOW PRESSURE GAS STREAMS FDA UDI
Model / Reference
28032 FDA UDI
Description
GAS COLLECTING VESSEL, COLLECT AND STORE GAS SAMPLES OR LOW PRESSURE GAS STREAMS FDA UDI

Identifiers

Primary DI / UDI-DI
06950471300151 FDA UDI
FDA Product Code
KGK FDA UDI
GMDN Term
Exhaled-gas sample collector, non-electronic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.1575 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Exhaled-gas sample collector, non-electronic

Gas Collecting Vessel by Hangzhou A-Tek Medical & Textiles Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exhaled-gas sample collector, non-electronic.

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

Sources (1)

  • FDA UDI 59183742-17e6-494a-8939-6959c54e6c86 33 fields · synced Jun 8, 2026