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Surustap

by Suru International Pvt Ltd

Ref 1018

Surustap (1018) is a Class IIa device made by Suru International Pvt Ltd, registered in EUDAMED on 17 Jun 2026 (Basic UDI-DI 89021411018PM), active as of 7 Nov 2026.

Active European Union

CE MDR CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number89021411018PM Basic UDI-DI 08902141103331UDI-DIDate17 Jun 2026RegisteredStatusActive
European UnionCE/MDR Number89021411018PM Basic UDI-DI 08902141103331UDI-DIDate17 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Device name
Skin Stapler
Model / reference
1018
Primary DI / UDI-DI
08902141103331
Basic UDI-DI
89021411018PM, B-08902141103331
EMDN code
H02010101 Skin staplers, single-use
Device class
Class IIa
System or procedure pack
System which is a device in itself
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IN-MF-000023736
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Similar devices in this category

Other devices filed under SKIN STAPLERS, SINGLE-USE.

Other devices from Suru International Pvt Ltd

See all devices from Suru International Pvt Ltd →

Properties

  • Supplied sterile
Other properties (13, all answered No)