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Exomine Regeneration Kit

EUDAMED

Class III (EU MDR)

Ref EM 9600

by T-Bi̇yoteknoloji̇ Laboratuvar Esteti̇k Medi̇kal Kozmeti̇k San. Ti̇c. Ltd. Şti̇.

Identity

Trade Name
EXOMINE REGENERATION KIT EUDAMED
Device Name
EXOMINE REGENERATION KIT EUDAMED
Model / Reference
EM 9600 EUDAMED

Identifiers

Primary DI / UDI-DI
08682754375799 EUDAMED
Basic UDI-DI
868275437EM9600GK EUDAMED
EMDN Code
V0599 CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class III EUDAMED
Medical Purpose
The indications for use of EXOMINE REGENERATIVE KIT are as follows: intra and subdermal injection for the correction of fine wrinkles, intra and subdermal injection for the correction of sun damage, intra and subdermal injection for the correction of skin color, subdermal injection for the revitalization of hair follicles and intra-articular injection for joint repair. EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

Exomine Regeneration Kit by T-Bi̇yoteknoloji̇ Laboratuvar Esteti̇k Medi̇kal Kozmeti̇k San. Ti̇c. Ltd. Şti̇. — Class III — MDR — listed in EUDAMED

Similar devices

Also classified as Ophthalmic surgical procedure kit, non-medicated, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
T-Bi̇yoteknoloji̇ Laboratuvar Esteti̇k Medi̇kal Kozmeti̇k San. Ti̇c. Ltd. Şti̇.
EUDAMED SRN
TR-PR-000016407

Sources (1)

  • EUDAMED 3d72c6f0-1861-4370-a063-3c3b52d6b7f0 61 fields · synced Oct 6, 2026