← Back to catalogue

Bemis

FDA UDI

Class II (US FDA UDI)

by Bemis Manufacturing Co.

Identity

Trade Name
Bemis FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
ONE-LINER STOPCOCK MANIFOLD - QUICK-FIT FDA UDI
Model / Reference
538110 FDA UDI
Description
ONE-LINER STOPCOCK MANIFOLD - QUICK-FIT FDA UDI

Identifiers

Catalog Number
538110 FDA UDI
Primary DI / UDI-DI
10073088150476 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

No

FDA UDI

Over-the-Counter

Yes

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

Bemis by Bemis Manufacturing Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 1755693c-412c-44fc-9cc2-fbb3e3859ed3 35 fields · synced May 30, 2026