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Surflo Midela MCS2208D01F

by Terumo Medical Products (Hangzhou) Co., Ltd.

Surflo Midela MCS2208D01F is a Class II device made by Terumo Medical Products (Hangzhou) Co., Ltd., listed in FDA GUDID since 1 Apr 2026 (UDI-DI 36927675517297), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number36927675517297 UDI-DI Date1 Apr 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Surflo Midela
Generic name
Peripheral vascular intervention infusion catheter
Model / Ref / Catalog
MCS2208D01F
Primary DI / UDI-DI
36927675517297
FDA product code
FOZ, PND
GMDN term
Peripheral vascular intervention infusion catheter
Device class
Class II
Regulation number
880.5200
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Length — 80 Millimeter
Catheter Gauge — 0.7 French

Other devices from Terumo Medical Products (Hangzhou) Co., Ltd.

See all devices from Terumo Medical Products (Hangzhou) Co., Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Combination product
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (7, all answered No)