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SteroScope Insert Connector Large Assembly, Type 2, Qty 1 02-207033-002

by Ideate Medical

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

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 Number00850043134282 UDI-DI Date30 Jun 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
SteroScope Insert Connector Large Assembly, Type 2, Qty 1
Generic Name
Luminal device flushing tubing set, single-use
Model / Reference
02-207033-002
Primary DI / UDI-DI
00850043134282
510(k) Number
FDA Product Code
MLR
GMDN Term
Luminal device flushing tubing set, single-use
Device Class
Class II
Regulation Number
880.6860
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K233762)

Show all (12)

Other devices from Ideate Medical

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Properties

  • Single Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: 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
  • Serial Number: No
  • Expiration Date: No