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Ophidia Vacuum Heart Stabilizer STB-900VS

by Kdl Medical, Inc.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00899054002869 UDI-DI Date13 Aug 2026ListedStatusListed 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  • Withdrawn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
Ophidia Vacuum Heart Stabilizer
Generic Name
Patient positioning vacuum pad
Model / Reference
STB-900VS
Primary DI / UDI-DI
00899054002869
FDA Product Code
MWS
GMDN Term
Patient positioning vacuum pad
Device Class
Class I
Regulation Number
870.4500
GUDID distribution status
In Commercial Distribution

Other devices from Kdl Medical, Inc.

See all devices from Kdl Medical, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No