Skip to content

Perouse Medical 3015SPIMST

by Perouse Medical

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 Number03661234027484 UDI-DI Date22 Jan 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  • Withdrawn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
Perouse Medical
Generic Name
Vascular port/catheter
Model / Ref / Catalog
3015SPIMST, VPE3015SPIMST
Primary DI / UDI-DI
03661234027484
510(k) Number
FDA Product Code
LJT
GMDN Term
Vascular port/catheter
Device Class
Class II
Regulation Number
880.5965
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K122834)

Show all (12)

Other devices from Perouse Medical

See all devices from Perouse Medical →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • 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
  • Manufacturing Date: No