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SonoBlock

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name
SonoBlock FDA UDI
Generic Name
Peripheral nerve-block sharp needle FDA UDI
Device Name
SonoBlock 22G (0,70) x 50mm with injection tube FDA UDI
Model / Reference
001180-31G FDA UDI
Description
SonoBlock 22G (0,70) x 50mm with injection tube FDA UDI

Identifiers

Catalog Number
001180-31G FDA UDI
Primary DI / UDI-DI
04048223130476 FDA UDI
510(k) Number
K111374 FDA UDI
K241954 FDA UDI
FDA Product Code
BSP FDA UDI
GMDN Term
Peripheral nerve-block sharp 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

Category: Peripheral nerve-block sharp needle

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

Similar devices

Also classified as Peripheral nerve-block sharp needle.

Cleared under the same submission

K111374 also covers:

K241954 also covers:

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 4d31c0d0-a4ff-4a39-9352-dcf5a4463e4a 37 fields · synced May 30, 2026