Skip to content

Integra® Dermal Regeneration Template

by Integra LifeSciences Corporation 14 variants

Ref 68101T

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-10381780356271 Basic UDI-DI 10381780356271UDI-DIDate10 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicAustriaHungaryRomaniaPortugalSpainItalyGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

EU market availability

Made available in 22 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 25 May 2011
  • Belgium since 25 May 2011
  • Cyprus since 25 May 2011
  • Czechia since 25 May 2011
  • Denmark since 25 May 2011
  • Estonia since 25 May 2011
  • Finland since 25 May 2011
  • France since 25 May 2011
  • Germany since 25 May 2011
  • Greece since 25 May 2011
  • Hungary since 25 May 2011
  • Ireland since 25 May 2011
  • Italy since 25 May 2011
  • Latvia since 25 May 2011
  • Luxembourg since 25 May 2011
  • Malta since 25 May 2011
  • Netherlands since 25 May 2011
  • Poland since 25 May 2011
  • Portugal since 25 May 2011
  • Romania since 25 May 2011
  • Spain since 25 May 2011
  • Sweden since 25 May 2011

Last checked 25 Oct 2026.

Specification

EUDAMED

Device Name
Integra Meshed Dermal Regeneration Template, Integra Dermal Regeneration Template - Terminally Sterilized, Single Layer, Thin
Model / Reference
68101T
Primary DI / UDI-DI
10381780356271
Basic UDI-DI
B-10381780356271
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
US-MF-000007196
Authorised representative
Integra LifeSciences Services FR-AR-000002474

Other devices from Integra Lifesciences Corp.

See all devices from Integra Lifesciences Corp. →

Properties

  • Sterile
  • Implantable
  • Animal Tissues

Other properties (10)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No