← Back to catalogue

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
001180-30G FDA UDI
Model / Reference
001180-30G FDA UDI
Description
001180-30G FDA UDI

Identifiers

Catalog Number
001180-30G FDA UDI
Primary DI / UDI-DI
04048223050583 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
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

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

No

FDA UDI

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

Cleared under the same submission

K111374 also covers:

K241954 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Pajunk GmbH Medizintechnologie

Sources (1)

  • FDA UDI f3a4fd67-3427-4712-9ae8-73a4d95dcdd9 38 fields · synced May 31, 2026