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Rftl 001165-30BM

by Pajunk GmbH Medizintechnologie GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04048223131282 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  • Withdrawn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
Rftl
Generic Name
Percutaneous radio-frequency ablation probe cannula, single-use
Model / Ref / Catalog
001165-30BM
Primary DI / UDI-DI
04048223131282
510(k) Number
FDA Product Code
GXI
GMDN Term
Percutaneous radio-frequency ablation probe cannula, single-use
Device Class
Class II
Regulation Number
882.4725
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K060397)

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