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RetroPerc RP91-01

by Retroperc, Inc.

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 Number00860000917506 UDI-DI Date9 Jan 2025ListedStatusListed 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  • Withdrawn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
RetroPerc
Generic Name
Nephrostomy introduction sheath
Model / Ref / Catalog
RP91-01
Primary DI / UDI-DI
00860000917506
FDA Product Code
LJE
GMDN Term
Nephrostomy introduction sheath
Device Class
U
GUDID distribution status
In Commercial Distribution

Related devices

Category: Nephrostomy introduction sheath

Similar devices

Also classified as Nephrostomy introduction sheath.

Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration 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
  • Serial Number: No
  • Manufacturing Date: No