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SureSigns VM8SE SureSigns VM8 SE Patient Monitor

by Philips Medical Systems Hsg

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00884838050464 UDI-DI Date3 Oct 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
SureSigns VM8SE
Generic Name
General-purpose multi-parameter bedside monitor
Model / Ref / Catalog
SureSigns VM8 SE Patient Monitor, 863317
Primary DI / UDI-DI
00884838050464
FDA Product Code
MHX
GMDN Term
General-purpose multi-parameter bedside monitor
Device Class
Class II
Regulation Number
870.1025
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Related devices

Category: General-purpose multi-parameter bedside monitor

Other devices from Philips Medical Systems Hsg

See all devices from Philips Medical Systems Hsg →

Properties

  • Prescription Use
  • Serial Number

Other properties (12)

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