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RegenET

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref R-ET-3 x 10

by Regen Lab SA

Identity

Trade Name
RegenET EUDAMEDFDA UDI
Generic Name
Haematological concentrate system preparation kit, platelet concentration FDA UDI
Device Name
RegenET EUDAMED
Model / Reference
R-ET-3 x 10 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
07640138981487 EUDAMEDFDA UDI
Basic UDI-DI
B-07640138981487 EUDAMED
FDA Product Code
KJC FDA UDI
EMDN Code
B06 CELLULAR OR BIOLOGICAL MANIPULATION DEVICES EUDAMED
GMDN Term
Haematological concentrate system preparation kit, platelet concentration FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
864.2240 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

RegenET by Regen Lab Sa — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Regen Lab SA
EUDAMED SRN
CH-MF-000032231
Authorised Representative
RegenLab France FR-AR-000011953

Sources (2)

  • EUDAMED 57b03d08-7633-43c3-8417-4f580b0d0df1 61 fields · synced Jun 20, 2026
  • FDA UDI 0f4bf808-62d5-4bda-9579-e53be6568ccc 33 fields · synced May 30, 2026