← Back to catalogue

Acetabular reamer Ø51 with round tooth

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref T17808Model Acetabular reamerRef T18224

by MPS Micro Precision Systems AG

Identity

Trade Name
Acetabular reamer Ø51 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
T17808 EUDAMEDFDA UDI
T18224 EUDAMEDFDA UDI
Description
Acetabular reamer for hip arthroplasty FDA UDI

Identifiers

Catalog Number
T17808 FDA UDI
T18224 FDA UDI
Primary DI / UDI-DI
07640187912890 EUDAMEDFDA UDI
07640187912449 EUDAMEDFDA UDI
Basic UDI-DI
764018791REAMACETAB01SP 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 Ø51 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

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 ed9f2d99-6f5e-4b41-b5be-f3621847f5cf 61 fields · synced Jul 8, 2026
  • FDA UDI 605c12ef-0b95-49e4-a33b-e86caed91c81 35 fields · synced May 29, 2026
  • FDA UDI 05c0064e-aa01-4d17-a3ea-da701e644632 35 fields · synced May 30, 2026
  • EUDAMED 15dee397-affb-41f5-8182-1b7f424c6fca 61 fields · synced Jul 8, 2026