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Reavillmed, LLC 660925B

by Reavillmed

Listed FDA GUDID listing, not in commercial distribution

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 Number00863523000304 UDI-DI Date27 Dec 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Reavillmed, LLC
Generic Name
Invasive blood pressure monitoring tubing set
Model / Reference
660925B
Primary DI / UDI-DI
00863523000304
FDA Product Code
LJS, DRS
GMDN Term
Invasive blood pressure monitoring tubing set
Device Class
Class II
Regulation Number
880.5970, 870.2850
GUDID distribution status
Not in Commercial Distribution

Other devices from Reavillmed

Properties

  • Sterile
  • Single Use
  • Lot / Batch Number

Other properties (11)

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