Skip to content

UniPlex® Nanoline® 001156-82

by Pajunk GmbH Medizintechnologie GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04048223130124 UDI-DIDate4 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  • Withdrawn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
UniPlex® Nanoline®
Generic Name
Nerve-locating anaesthesia needle
Model / Ref / Catalog
001156-82
Primary DI / UDI-DI
04048223130124
510(k) Number
FDA Product Code
BSP
GMDN Term
Nerve-locating anaesthesia needle
Device Class
Class II
Regulation Number
868.5150
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 0.7 Millimeter
Length — 120.0 Millimeter

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