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Acetabular reamer Ø60 with round tooth

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref T17817Model Acetabular reamerRef T18233

by MPS Micro Precision Systems AG

Identity

Trade Name
Acetabular reamer Ø60 with round tooth EUDAMEDFDA UDI
Generic Name
Acetabular orthopaedic reamer FDA UDI
Device Name
Acetabular reamer for hip arthroplasty FDA UDI
Model / Reference
Acetabular reamer EUDAMED
T17817 EUDAMEDFDA UDI
T18233 EUDAMEDFDA UDI
Description
Acetabular reamer for hip arthroplasty FDA UDI

Identifiers

Catalog Number
T18233 FDA UDI
T17817 FDA UDI
Primary DI / UDI-DI
07640187912982 EUDAMEDFDA UDI
07640187912531 EUDAMEDFDA UDI
Basic UDI-DI
764018791REAMACETAB01SP EUDAMED
Direct Marketing DI
07640187912982 EUDAMED
07640187912531 EUDAMED
FDA Product Code
HTO FDA UDI
EMDN Code
L091102 ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE EUDAMED
GMDN Term
Acetabular orthopaedic reamer 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 UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Acetabular orthopaedic reamer

Acetabular reamer Ø60 with round tooth 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

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Manufacturer

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

Sources (4)

  • EUDAMED 8c2f7f1e-c03f-4f04-b8d3-1fc65d3dd98c 61 fields · synced Jul 12, 2026
  • FDA UDI 5076b41d-aa2a-44c1-8224-cbbe5d8049b0 35 fields · synced May 30, 2026
  • FDA UDI ba9f3d8a-b7ee-48c7-bf7f-42d6752b27ec 35 fields · synced May 30, 2026
  • EUDAMED 6ed1da7a-885f-489b-ade2-30c3fd32f840 61 fields · synced Jul 12, 2026