Flowtube Hf

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name: FLOWTUBE HF FDA UDI
Generic Name: Haemostatic knife FDA UDI
Device Name: 1299-01-15 FDA UDI
Model / Reference: 1299-01-15 FDA UDI
Description: 1299-01-15 FDA UDI

Identifiers

Catalog Number: 1299-01-15 FDA UDI
Primary DI / UDI-DI: 04048223083673 FDA UDI
FDA Product Code: GEI FDA UDI
GMDN Term: Haemostatic knife FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4400 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Haemostatic knife

Flowtube Hf by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Pajunk GmbH Medizintechnologie

Sources (1)

FDA UDI 37efde4d-9e31-4a4a-8823-39cffeabd500 36 fields · synced May 30, 2026