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Radius and Ulnar Locking Plate, pure titanium

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 020722003

by Double Medical Technology Inc.

Identity

Trade Name
Distal Radius Locking Plate II, Combi-holes FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
Radius and Ulnar Locking Plate, pure titanium EUDAMED
Model / Reference
020722003 EUDAMEDFDA UDI

Identifiers

Catalog Number
020722003 FDA UDI
Primary DI / UDI-DI
06942782475642 EUDAMEDFDA UDI
Basic UDI-DI
6902139CS03005AX EUDAMED
510(k) Number
K130108 FDA UDI
FDA Product Code
HRS FDA UDI
HWC FDA UDI
EMDN Code
P09120501 OSTEOSYNTHESIS COMPRESSION PLATES 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
888.3040 FDA UDI
Market of Registration
Lithuania EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 49.9 Millimeter FDA UDI
Width — 9.0 Millimeter FDA UDI

Radius and Ulnar Locking Plate, pure titanium by Double Medical Technology Inc. — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CN-MF-000009048
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED bfb1a768-3447-4fa1-8aee-97c2f9d10fff 61 fields · synced Jul 19, 2026
  • FDA UDI 398db72b-be0d-4954-bc8e-c6ea5adbb4e5 36 fields · synced May 30, 2026