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Sea-Long Medical Hood 500 Seris Model

by Sea-Long Medical Systems, 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850052737009 UDI-DI Date21 Nov 2024ListedStatusListed 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  • Withdrawn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
Sea-Long Medical Hood
Generic Name
Oxygen administration hood, adult
Model / Reference
500 Seris Model
Primary DI / UDI-DI
00850052737009
FDA Product Code
FOG, CBF
GMDN Term
Oxygen administration hood, adult
Device Class
Class I
Regulation Number
868.5700, 868.5470
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ultraviolet Light

Related devices

Category: Oxygen administration hood, adult

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Properties

  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • 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