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Ceeport 63134B-SK

by Ceeport 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 Number00850087488808 UDI-DI Date26 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  • Withdrawn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
Ceeport
Generic Name
Compression/pressure tubular garment
Model / Reference
63134B-SK
Primary DI / UDI-DI
00850087488808
FDA Product Code
FQM
GMDN Term
Compression/pressure tubular garment
Device Class
Class I
Regulation Number
880.5075
GUDID distribution status
In Commercial Distribution

Other devices from Ceeport inc.

See all devices from Ceeport inc. →

Properties

  • Contains Latex
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No