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Flow Tap

FDA UDI

Class I (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name
FLOW TAP FDA UDI
Generic Name
Stopcock FDA UDI
Device Name
Flowtap. flow 2.9mm, right, FDA UDI
Model / Reference
1280-03WR FDA UDI
Description
Flowtap. flow 2.9mm, right, FDA UDI

Identifiers

Catalog Number
1280-03WR FDA UDI
Primary DI / UDI-DI
04048223111512 FDA UDI
FDA Product Code
KOA FDA UDI
GMDN Term
Stopcock FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Stopcock

Flow Tap by Pajunk GmbH Medizintechnologie — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stopcock.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI afc084e6-9c47-4015-aff1-4865448c1691 34 fields · synced May 31, 2026