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Curaplex 301-FO-MIL-000

by Bound Tree Medical, LLC

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 2 Nov 2026. What this means

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810071638688 UDI-DI Date21 Oct 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  • Withdrawn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
Curaplex
Generic Name
Laryngoscope blade, reusable
Model / Ref / Catalog
301-FO-MIL-000
Primary DI / UDI-DI
00810071638688
FDA Product Code
CCW
GMDN Term
Laryngoscope blade, reusable
Device Class
Class I
Regulation Number
868.5540
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide

Other devices from Bound Tree Medical, LLC

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt

Other properties (10)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No