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Reefan MM0521

by Zhangzhou Easepal Medical Science And Technology Co., 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 Number06974989947509 UDI-DI Date6 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  • Withdrawn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
Reefan
Generic Name
Intermittent venous compression system
Model / Reference
MM0521
Primary DI / UDI-DI
06974989947509
510(k) Number
FDA Product Code
ILO
GMDN Term
Intermittent venous compression system
Device Class
Class II
Regulation Number
890.5720
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K240373)

Other devices from Zhangzhou Easepal Medical Science And Technology Co., Ltd.

Properties

  • Lot / Batch Number

Other properties (13)

  • Sterile: No
  • Single Use: 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
  • Manufacturing Date: No