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Patient Monitoring Cable (SpO2 Extension Cable) CR002-5301

by Shenzhen Coreray Technology, Ltd.

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 Number06928737818146 UDI-DI Date11 May 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  • Withdrawn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
Patient Monitoring Cable (SpO2 Extension Cable)
Generic Name
Electrical-only medical device connection cable, reusable
Model / Reference
CR002-5301
Primary DI / UDI-DI
06928737818146
510(k) Number
FDA Product Code
DSA
GMDN Term
Electrical-only medical device connection cable, reusable
Device Class
Class II
Regulation Number
870.2900
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • 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
  • Serial Number: No
  • Expiration Date: No