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M-Drain D11014030S

by Mermaid Medical A/S

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number15711055003244 UDI-DIDate4 Sep 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  • Withdrawn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
M-Drain
Generic Name
Multi-purpose percutaneous abdominothoracic drainage catheter
Model / Ref / Catalog
D11014030S
Primary DI / UDI-DI
15711055003244
FDA Product Code
FGE
GMDN Term
Multi-purpose percutaneous abdominothoracic drainage catheter
Device Class
Class II
Regulation Number
876.5010
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe
Size
Length — 15 Centimeter
Catheter Gauge — 6 French

Other devices from Mermaid Medical A/S

See all devices from Mermaid Medical A/S →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No