Filter cannula NRFit

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name: Filter cannula NRFit FDA UDI
Generic Name: Anaesthesia conduction filter FDA UDI
Device Name: Filter cannula NRFit 18G x 50mm, sterile FDA UDI
Model / Reference: 001163-38Y FDA UDI
Description: Filter cannula NRFit 18G x 50mm, sterile FDA UDI

Identifiers

Catalog Number: 001163-38Y FDA UDI
Primary DI / UDI-DI: 04048223070598 FDA UDI
510(k) Number: K172777 FDA UDI
FDA Product Code: BSO FDA UDI
GMDN Term: Anaesthesia conduction filter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5120 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size: Needle Gauge — 18.0 Gauge FDA UDI
Length — 50.0 Millimeter FDA UDI

Category: Anaesthesia conduction filter

Filter cannula NRFit by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K172777 also covers:

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 125a1b27-f82d-4534-9474-6cf0c30e02f3 38 fields · synced Jun 7, 2026