← Back to catalogue

Humeral IM reamer Ø7.5 x 343 mm, can. Ø2.3 mm, Big AO coup.

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref T4869Model IM Reamer MonoblocRef T13672

by MPS Micro Precision Systems AG

Identity

Trade Name
Humeral IM reamer Ø7.5 x 343 mm, can. Ø2.3 mm, Big AO coup. EUDAMEDFDA UDI
Humeral IM reamer Ø7.5 x 343 mm, can. Ø2.3 mm Hudson coup. EUDAMEDFDA UDI
Generic Name
Medullary canal orthopaedic reamer, flexible FDA UDI
Device Name
Humeral monobloc intramedullary reamer is used to ream the medullary cavity of humeral bone prior to placing a nail. A range of diameter is proposed in regards with the nail to be implanted and a range of length is proposed in regards with the height of the bone. Different distal coupling are available to connect with existing power tool. This is a reusable device. FDA UDI
Model / Reference
IM Reamer Monobloc EUDAMED
T4869 EUDAMEDFDA UDI
T13672 EUDAMEDFDA UDI
Description
Humeral monobloc intramedullary reamer is used to ream the medullary cavity of humeral bone prior to placing a nail. A range of diameter is proposed in regards with the nail to be implanted and a range of length is proposed in regards with the height of the bone. Different distal coupling are available to connect with existing power tool. This is a reusable device. FDA UDI

Identifiers

Catalog Number
T4869 FDA UDI
T13672 FDA UDI
Primary DI / UDI-DI
07640187911398 EUDAMEDFDA UDI
07640187917802 EUDAMEDFDA UDI
Basic UDI-DI
764018791IMREAMMONO01DH EUDAMED
Direct Marketing DI
07640187917802 EUDAMED
FDA Product Code
HTO FDA UDI
EMDN Code
L091102 ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE EUDAMED
GMDN Term
Medullary canal orthopaedic reamer, flexible FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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 UDIFDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Acetabular orthopaedic reamer

Humeral IM reamer Ø7.5 x 343 mm, can. Ø2.3 mm, Big AO coup. by MPS Micro Precision Systems AG — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Acetabular orthopaedic reamer.

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
CH-MF-000032439
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (4)

  • EUDAMED 197fd27b-d03d-42f0-a034-31be5cde8017 61 fields · synced Jul 19, 2026
  • FDA UDI c10e3de3-e147-477d-a69f-fc72f5423683 35 fields · synced May 30, 2026
  • FDA UDI 044005a5-47b6-404c-8629-cc8c10437055 34 fields · synced May 30, 2026
  • EUDAMED 8566335b-1148-4576-be78-dac6d94be516 61 fields · synced Jul 19, 2026