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Posterior Glenoid Retractor

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 903-0055

by FX Shoulder Solutions

Identity

Trade Name
POSTERIOR GLENOID RETRACTOR EUDAMED
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
RETRACTOR EUDAMED
POSTERIOR GLENOID RETRACTOR FDA UDI
Model / Reference
903-0055 EUDAMED
903-0054 FDA UDI
Description
POSTERIOR GLENOID RETRACTOR FDA UDI

Identifiers

Catalog Number
903-0054 FDA UDI
Primary DI / UDI-DI
03701037312391 EUDAMEDFDA UDI
Basic UDI-DI
37010373RETRACTORCF EUDAMED
Direct Marketing DI
03701037312391 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L0915 SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, REUSABLE EUDAMED
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Italy 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Posterior Glenoid Retractor by FX Shoulder Solutions — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
FR-MF-000000465

Sources (2)

  • EUDAMED b2e6b297-efb2-415f-8394-fca916fef803 61 fields · synced Jun 19, 2026
  • FDA UDI 0ab084ba-1c5a-436c-a4c2-b621f2534745 35 fields · synced May 30, 2026