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Inion BioRestore™

EUDAMEDFDA UDI

Class III (EU MDR)

Ref BRS-5445

by Inion Oy

Identity

Trade Name
Inion BioRestore™ EUDAMED
Inion BioRestore™ FDA UDI
Generic Name
Synthetic bone graft FDA UDI
Device Name
Inion BioRestore EUDAMED
Morsels 2.0 cc FDA UDI
Model / Reference
BRS-5445 EUDAMED
1 FDA UDI
Description
Morsels 2.0 cc FDA UDI

Identifiers

Catalog Number
BRS-5445 FDA UDI
Primary DI / UDI-DI
06438408009136 EUDAMEDFDA UDI
Basic UDI-DI
B-06438408009136 EUDAMED
FDA Product Code
MQV FDA UDI
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED
GMDN Term
Synthetic bone graft FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
888.3045 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Inion BioRestore™ by Inion Oy — Class III — 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
Inion Oy
EUDAMED SRN
FI-MF-000000646

Sources (2)

  • EUDAMED e140acdb-3207-4e51-a469-7be70036f3a0 61 fields · synced Jul 12, 2026
  • FDA UDI 01a5b4fe-b3cd-43e3-9017-d2590a461c75 34 fields · synced May 30, 2026