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StimuLong Sono II NanoLine® 521187-32A

by Pajunk GmbH Medizintechnologie

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04048223126578 UDI-DI Date6 Nov 2025ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
StimuLong Sono II NanoLine®
Generic Name
Peripheral anaesthesia catheter set, non-medicated
Model / Ref / Catalog
521187-32A
Primary DI / UDI-DI
04048223126578
510(k) Number
FDA Product Code
CAZ
GMDN Term
Peripheral anaesthesia catheter set, non-medicated
Device Class
Class II
Regulation Number
868.5140
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K113188)

Show all (11)

Other devices from Pajunk GmbH Medizintechnologie

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Properties

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

Other properties (9)

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