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PWC101

by Medtronic, Inc.

PWC101 is a Class III device made by Medtronic, Inc., approved under FDA PMA P230017 on 13 Dec 2023 and listed in FDA GUDID since 5 Feb 2024 (UDI-DI 00763000642082), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

PMA

Valid until

No expiry

PMA approval is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

PMA P230017

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00763000642082 UDI-DI Date5 Feb 2024ListedStatusListed GUDID: in commercial distribution
United StatesFDA PMAAPPR from GUDID Approved NumberP230017 Date13 Dec 2023DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA PMA P230017 decided 13 Dec 2023 Active
  • FDA GUDID UDI-DI 00763000642082 listed 5 Feb 2024 Listed

Timeline

2 dated events

  1. Approved FDA PMA P230017
  2. Listed FDA GUDID 00763000642082

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA PMA Active

Specification

GUDID

Generic name
Electrical mains power cable
Model / reference
PWC101
Primary DI / UDI-DI
00763000642082
PMA number
FDA product code
QZI
GMDN term
Electrical mains power cable
Device class
Class III
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrical mains power cable

Cleared under the same submission (P230017)

and 1 more cleared under P230017

Similar devices in this category

Other devices filed under Electrical mains power cable.

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)