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Laminate Medical Technologies Ltd.

Certificate 3903065CE01

Rev. 2Amended
Valid until
Jan 1, 2031

Certificate 3903065CE01 is a valid Quality management system issued to Laminate Medical Technologies Ltd. and registered in EUDAMED. Valid until January 1, 2031. View the full certificate record on MD Atlas.

Overview

Certificate number
3903065CE01
Certificate type
Quality management system
Certificate status
Amended
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
03443903065CE012

Validity

Issued
May 11, 2026
Valid from
May 11, 2026
Valid until
Jan 1, 2031

Notified body

Notified body
DEKRA Certification B.V.
Notified body SRN
0344
Notified body country
Netherlands

Characteristics

Sterile
Yes
Human tissues
No
Animal tissues
No
In vitro diagnostics
No
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
No
Mechanism of scrutiny
No
Intended medical purpose
No
SPP applicable
No
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Basic UDI-DI data only

History

Status changes

  • Amended

Supersedes

  • 3903065CE01AmendedJan 12, 2026 → Jan 1, 2031

Predecessor certificate not registered in EUDAMED.

Scope coverage

Class IIa1Class IIb1

2 scopes

  • DEVICE
    Class IIa
  • DEVICE
    Class IIb

Documents

LanguagesEN

Manufacturer

Manufacturer
Laminate Medical Technologies Ltd.
Manufacturer SRN
IL-MF-000009312
Manufacturer country
Israel

Covered devices

  • Disposable Model Selection Tool (DMST)Class IIa
    7290016063DMSTEU62
  • VasQClass IIb
    7290016063VasQEUPX