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Resolve Modular Revision Stem

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 9112-3620

by United Orthopedic Corporation

Identity

Trade Name
Resolve Modular Revision Stem EUDAMEDFDA UDI
Generic Name
Medullary canal orthopaedic reamer, rigid FDA UDI
Device Name
Resolve taper reamer, Ø20×180mm EUDAMEDFDA UDI
Model / Reference
9112-3620 EUDAMEDFDA UDI
Description
Resolve taper reamer, Ø20×180mm FDA UDI

Identifiers

Catalog Number
9112-3620 FDA UDI
Primary DI / UDI-DI
04719886902679 EUDAMEDFDA UDI
Basic UDI-DI
B-04719886902679 EUDAMED
FDA Product Code
HTO FDA UDI
EMDN Code
L091102 ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE EUDAMED
GMDN Term
Medullary canal orthopaedic reamer, rigid FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
France 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

Resolve Modular Revision Stem by United Orthopedic Corporation — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabular orthopaedic reamer.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
TW-MF-000009523
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (2)

  • EUDAMED 0c1d4ce2-60d8-44f8-9d49-ac0f08083bba 61 fields · synced Jun 9, 2026
  • FDA UDI 2efaccc3-9051-49b8-a38c-635f8593b19c 35 fields · synced May 30, 2026