← Back to catalogue

MorSafe Tissue Morcellation Bag

EUDAMED

Class IIa (EU MDR)

Ref XG-500-MModel XG-500Ref XG-500-S

by Veol Medical Technologies Pvt. Ltd.

Identity

Device Name
MorSafe Tissue Morcellation Bag EUDAMED
Model / Reference
XG-500 EUDAMED
XG-500-M EUDAMED
XG-500-S EUDAMED

Identifiers

Primary DI / UDI-DI
08906138880359 EUDAMED
08906138880366 EUDAMED
Basic UDI-DI
890613888XG3B EUDAMED
EMDN Code
Z12080204 MORCELLATORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

MorSafe Tissue Morcellation Bag by Veol Medical Technologies Pvt. Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IN-MF-000007679
Authorised Representative
Mars Medical DE-AR-000006312

Sources (2)

  • EUDAMED 37679f73-f7ad-4b7d-97ca-6ec840e99e0c 61 fields · synced Jul 26, 2026
  • EUDAMED f05e2955-bf89-42bb-ae73-04a1e3df0bf7 61 fields · synced May 18, 2026