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UniPlex

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name
UniPlex FDA UDI
Generic Name
Nerve-locating anaesthesia needle FDA UDI
Device Name
UniPlex UP 3/40, 0,70 x 40mm, Facetten-Tip, with injection tubing + connecting cable FDA UDI
Model / Reference
001153-70 FDA UDI
Description
UniPlex UP 3/40, 0,70 x 40mm, Facetten-Tip, with injection tubing + connecting cable FDA UDI

Identifiers

Catalog Number
001153-70 FDA UDI
Primary DI / UDI-DI
14048223019501 FDA UDI
FDA Product Code
BSP FDA UDI
GMDN Term
Nerve-locating anaesthesia needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5150 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6df122d7-d2cb-4241-986b-cef700f06e8e 36 fields · synced Jun 1, 2026