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Bio Centric Inc BP900SiM

by Bio Centric Inc. GUDID

Listed (no authorization) FDA GUDID database listing only

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860005485802 UDI-DIDate1 Dec 2020ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Bio Centric Inc
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Model / Reference
BP900SiM
Primary DI / UDI-DI
00860005485802
FDA Product Code
NPP
GMDN Term
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Device Class
Class II
Regulation Number
870.1120
Commercial Distribution
In Commercial Distribution

Related devices

Category: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

Properties

  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No