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Dual Chamber Warming Cabinet FHCDWC2460-Tl-D

by M.A.C. Medical Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 NumberB286FHCDWC2460TLD1 UDI-DI Date27 Jul 2016ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Dual Chamber Warming Cabinet
Generic Name
Blanket warming cabinet, dry-heat
Model / Ref / Catalog
FHCDWC2460-TL-D
Primary DI / UDI-DI
B286FHCDWC2460TLD1
510(k) Number
FDA Product Code
LHC
GMDN Term
Blanket warming cabinet, dry-heat
Device Class
Class I
Regulation Number
890.5950
GUDID distribution status
In Commercial Distribution

Other devices from M.A.C. Medical Inc.

See all devices from M.A.C. Medical Inc. →

Properties

  • Serial Number

Other properties (13)

  • 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
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No