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Lead Adapter 501203

by Greatbatch Ltd

Lead Adapter 501203 is a Class II device made by Greatbatch Ltd, listed in FDA GUDID since 16 Oct 2015 (UDI-DI 00821329900235), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00821329900235 UDI-DI Date16 Oct 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Lead Adapter
Generic name
Pacing/defibrillation lead electrical adaptor
Model / reference
501203
Primary DI / UDI-DI
00821329900235
FDA product code
DTD
GMDN term
Pacing/defibrillation lead electrical adaptor
Device class
Class II
Regulation number
870.3620
GUDID distribution status
In Commercial Distribution
Size
Length — 13 Centimeter
Lumen/Inner Diameter — 4.75 Millimeter

Related devices

Category: Pacing/defibrillation lead electrical adaptor

Similar devices

Also classified as Pacing/defibrillation lead electrical adaptor.

Other devices from Greatbatch Ltd

See all devices from Greatbatch Ltd →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Convenience kit
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)