← Back to catalogue

Dispenser for K-wire 200 mm

EUDAMEDFDA UDI

Class I (EU MDR)

Ref UKWI00200T

by BRM Extremities S.r.l.

Identity

Trade Name
Dispenser for K-wire 200 mm EUDAMED
BRM TOOL SCREW INSTRUMENT FDA UDI
Generic Name
Orthopaedic bone pin container FDA UDI
Device Name
Dispositivi non invasivi di classe I accessori alle Viti per Osteosintesi EUDAMED
Model / Reference
UKWI00200T EUDAMED
Dispenser for K-wire 200mm FDA UDI

Identifiers

Catalog Number
UKWI00200T FDA UDI
Primary DI / UDI-DI
08057717553345 EUDAMEDFDA UDI
Basic UDI-DI
805771755FT07C1BU EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS EUDAMED
GMDN Term
Orthopaedic bone pin container FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Dispenser for K-wire 200 mm by BRM Extremities S.r.l. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

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

EUDAMED SRN
IT-MF-000016087

Sources (2)

  • EUDAMED bbd704ea-98b8-4ea2-bb64-e335cb34e848 61 fields · synced Jun 19, 2026
  • FDA UDI 5c077cfb-323e-47f7-b512-cbd56edfe97e 35 fields · synced May 30, 2026