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Perfusion Cannula PCAN8

by Institut Georges Lopez

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number13700911901024 UDI-DI Date11 May 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Perfusion Cannula
Generic Name
Kidney donor-organ preservation/transport perfusion set
Model / Reference
PCAN8
Primary DI / UDI-DI
13700911901024
510(k) Number
FDA Product Code
KDN
GMDN Term
Kidney donor-organ preservation/transport perfusion set
Device Class
Class II
Regulation Number
876.5880
GUDID distribution status
In Commercial Distribution
Size
Lumen/Inner Diameter — 8 Millimeter

Related devices

Cleared under the same submission (K211224)

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No