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Shengjie M1

by Weihai Shengjie Medical Technology Co., Ltd. 3 variants

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 Number06970614670354 UDI-DI Date2 Mar 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  • Withdrawn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
Shengjie
Generic Name
Oxygen administration tubing
Model / Reference
M1
Primary DI / UDI-DI
06970614670354
FDA Product Code
BZB
GMDN Term
Oxygen administration tubing
Device Class
Class I
Regulation Number
868.5350
GUDID distribution status
In Commercial Distribution

Other devices from Weihai Shengjie Medical Technology Co., Ltd.

See all devices from Weihai Shengjie Medical Technology Co., Ltd. →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

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