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Orthopaedic Surgical Instrument - Container

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 24-5905

by Buxton BioMedical, inc.

Identity

Trade Name
Buxton BioMedical FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Orthopaedic Surgical Instrument - Container EUDAMED
Steril.Case f/Shoulder Repair FDA UDI
Model / Reference
24-5905 EUDAMEDFDA UDI
Description
Steril.Case f/Shoulder Repair FDA UDI

Identifiers

Catalog Number
24-5905 FDA UDI
Primary DI / UDI-DI
+B7682459050C EUDAMED
B7682459050 FDA UDI
Basic UDI-DI
++B768TF5TM EUDAMED
Direct Marketing DI
+B7682459050C EUDAMED
FDA Product Code
FSM FDA UDI
EMDN Code
S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS EUDAMED
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Sweden 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Orthopaedic Surgical Instrument - Container by Buxton Biomedical, Inc. — 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

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Manufacturer

EUDAMED SRN
US-MF-000035059
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED 9bebc208-9a5a-41c7-83a9-e34e449fb587 61 fields · synced Jun 18, 2026
  • FDA UDI 9ddaaa3f-a794-486a-bab4-eb466904d8ec 34 fields · synced May 30, 2026