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BodyGuardian BG2002

by Boston Scientific Cardiac Diagnostic Technologies, Inc.

BodyGuardian BG2002 is a Class II device made by Boston Scientific Cardiac Diagnostic Technologies, Inc., listed in FDA GUDID since 7 Aug 2019 (UDI-DI 00852132007125), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00852132007125 UDI-DI Date7 Aug 2019ListedStatusListed 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  • Withdrawn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
BodyGuardian
Generic name
Medical networking interface unit
Model / reference
BG2002
Primary DI / UDI-DI
00852132007125
FDA product code
DSI
GMDN term
Medical networking interface unit
Device class
Class II
Regulation number
870.1025
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Medical networking interface unit

Similar devices in this category

Other devices filed under Medical networking interface unit.

Other devices from Boston Scientific Cardiac Diagnostic Technologies, Inc.

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Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)