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Surflash SR*FF1651

by Terumo Corp.

Part of a family of 12 devices: see the family page

Ref SR*FF1651

Surflash SR*FF1651 is a device classified as Class IIa in the EU and Class II in the US made by Terumo Corp., registered in EUDAMED on 31 Aug 2026 (Basic UDI-DI 498735037SRFFRC) and listed in FDA GUDID since 9 Sep 2016 (UDI-DI 34987350747755), active as of 24 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number498735037SRFFRC Basic UDI-DI 34987350747755UDI-DIDate31 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number34987350747755 UDI-DI Date9 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 498735037SRFFRC registered 31 Aug 2026 Active
  • FDA GUDID UDI-DI 34987350747755 listed 9 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 34987350747755
  2. Registered EUDAMED 498735037SRFFRC

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Surflash
Generic name
Peripheral intravenous cannula
Model / reference
SR*FF1651
Primary DI / UDI-DI
34987350747755
Basic UDI-DI
498735037SRFFRC
Unit of use DI
04987350747754
FDA product code
FOZ
EMDN code
C0101010102 Peripheral i.v. catheters, w/o safety systems, w/o injection valves
GMDN term
Peripheral intravenous cannula
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
880.5200
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Size
Length — 2 Inch

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Peripheral intravenous cannula

Similar devices in this category

Other devices filed under PERIPHERAL I.V. CATHETERS, W/O SAFETY SYSTEMS, W/O INJECTION VALVES.

Other devices from Terumo Corp.

See all devices from Terumo Corp. →

Properties

  • Supplied sterile
  • Single use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Administering medicine
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (17, all answered No)