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SonoMSK 1191-4E040

by Pajunk GmbH Medizintechnologie 2 variants

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number14048223036454 UDI-DI Date18 Oct 2018ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
SonoMSK
Generic Name
Peripheral nerve-block sharp needle
Model / Ref / Catalog
1191-4E040
Description
SonoMSK 22G x 40mm with Cornerstone Reflectors
Primary DI / UDI-DI
14048223036454
510(k) Number
FDA Product Code
BSP
GMDN Term
Peripheral nerve-block sharp needle
Device Class
Class II
Regulation Number
868.5150
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K113207)

Show all (11)

Other devices from Pajunk GmbH Medizintechnologie

See all devices from Pajunk GmbH Medizintechnologie →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No