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E-Cath® NRFit Tsui® 241165-40E

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 Number04048223086087 UDI-DI Date10 Jun 2026ListedStatusListed 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  • Withdrawn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
E-Cath® NRFit Tsui®
Generic Name
Peripheral anaesthesia catheter set, non-medicated
Model / Ref / Catalog
241165-40E
Primary DI / UDI-DI
04048223086087
510(k) Number
FDA Product Code
BSO
GMDN Term
Peripheral anaesthesia catheter set, non-medicated
Device Class
Class II
Regulation Number
868.5120
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe
Size
Needle Gauge — 21.0 Gauge
Catheter Gauge — 18.0 French
Length — 101.0 Millimeter

Related devices

Cleared under the same submission (K152952)

Show all (12)

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