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PlexoLong NanoLine® acc. Meier 531156-31A

by Pajunk GmbH Medizintechnologie GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04048223126394 UDI-DIDate6 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
PlexoLong NanoLine® acc. Meier
Generic Name
Peripheral anaesthesia catheter set, non-medicated
Model / Ref / Catalog
531156-31A
Primary DI / UDI-DI
04048223126394
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 (K053283)

Other devices from Pajunk GmbH Medizintechnologie

See all devices from Pajunk GmbH Medizintechnologie →

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