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SonoPlex® STIM

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name
SonoPlex® STIM FDA UDI
Generic Name
Nerve-locating anaesthesia needle FDA UDI
Device Name
SonoPlex® STIM 22G (0,70) x 40mm, with injection tube and connecting cable FDA UDI
Model / Reference
001185-70 FDA UDI
Description
SonoPlex® STIM 22G (0,70) x 40mm, with injection tube and connecting cable FDA UDI

Identifiers

Catalog Number
001185-70 FDA UDI
Primary DI / UDI-DI
04048223130247 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
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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.7 Millimeter FDA UDI
Length — 40.0 Millimeter FDA UDI

Category: Nerve-locating anaesthesia needle

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

Similar devices

Also classified as Nerve-locating anaesthesia needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pajunk GmbH Medizintechnologie

Sources (1)

  • FDA UDI 706362f1-f7c8-4956-aa73-ee0b0ac291cb 37 fields · synced Jun 8, 2026