← Back to catalogue

2.5 ADAPTIVE II TriLock DistRad.Pl Vol R

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref A-4750.108S

by Medartis AG

Identity

Trade Name
2.5 ADAPTIVE II TriLock DistRad.Pl Vol R EUDAMED
APTUS FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
Bone plates (sterile, non-sterile) EUDAMED
2.5 ADAPTIVE II TriLock DistRad.Pl Vol L FDA UDI
Model / Reference
A-4750.108S EUDAMED
A-4750.107S FDA UDI
Description
2.5 ADAPTIVE II TriLock DistRad.Pl Vol L FDA UDI

Identifiers

Catalog Number
A-4750.107S FDA UDI
Primary DI / UDI-DI
07630037890188 EUDAMEDFDA UDI
Basic UDI-DI
76300378020P6 EUDAMED
510(k) Number
K232144 FDA UDI
FDA Product Code
HRS FDA UDI
EMDN Code
P09120599 BONE FIXATION PLATES - OTHER EUDAMED
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Market of Registration
Germany 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

Sutures

Yes

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

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

Category: Orthopaedic fixation plate, non-bioabsorbable

2.5 ADAPTIVE II TriLock DistRad.Pl Vol R by Medartis AG — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Medartis AG
EUDAMED SRN
CH-MF-000022291
Authorised Representative
Medartis GmbH DE-AR-000005810

Sources (2)

  • EUDAMED a5822b9c-7ef7-4686-9c94-c80fbd778162 61 fields · synced Jun 19, 2026
  • FDA UDI 9c7fec2e-a83e-4ad9-8c1f-1cfd5ab6daa5 35 fields · synced May 30, 2026