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Sonolong Echo

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name
SONOLONG ECHO FDA UDI
Generic Name
Peripheral anaesthesia catheter set, non-medicated FDA UDI
Device Name
561185-31A FDA UDI
Model / Reference
561185-31A FDA UDI
Description
561185-31A FDA UDI

Identifiers

Catalog Number
561185-31A FDA UDI
Primary DI / UDI-DI
04048223117422 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Peripheral anaesthesia catheter set, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5140 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

No

FDA UDI

Category: Peripheral anaesthesia catheter set, non-medicated

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

Similar devices

Also classified as Peripheral anaesthesia catheter set, non-medicated.

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 fecabe33-2739-4cf3-8c21-77c1f2089a80 36 fields · synced Jun 6, 2026