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EpiLong Soft NRFit 1432167-51

by Pajunk GmbH Medizintechnologie

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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 Number04048223084366 UDI-DI Date21 May 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
EpiLong Soft NRFit
Generic Name
Epidural anaesthesia set, non-medicated
Model / Ref / Catalog
1432167-51
Primary DI / UDI-DI
04048223084366
FDA Product Code
OGD
GMDN Term
Epidural anaesthesia set, non-medicated
Device Class
Class II
Regulation Number
868.5120
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe
Size
Catheter Gauge — 20.0 French
Length — 90.0 Millimeter
Catheter Length — 900.0 Millimeter
Needle Gauge — 18.0 Gauge

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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