Skip to content

SPROTTE® NRFit 021163-29A

by Pajunk GmbH Medizintechnologie 2 variants

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 Number04048223127841 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  • Withdrawn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
SPROTTE® NRFit
Generic Name
Spinal needle, single-use
Model / Ref / Catalog
021163-29A
Primary DI / UDI-DI
04048223127841
510(k) Number
FDA Product Code
BSP
GMDN Term
Spinal needle, single-use
Device Class
Class II
Regulation Number
868.5150
GUDID distribution status
In Commercial Distribution
Size
Length — 90.0 Millimeter
Outer Diameter — 0.5 Millimeter

Related devices

Cleared under the same submission (K241953)

Show all (12)

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