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Humelock II Cemented Reversible Shoulder

FDA UDI

Class II (US FDA UDI)

by Fx Solutions

Identity

Trade Name
Humelock II Cemented Reversible Shoulder FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
TRIAL HUMERAL CUP 135/145° STANDARD Ø36 +9 FDA UDI
Model / Reference
913-0709 FDA UDI
Description
TRIAL HUMERAL CUP 135/145° STANDARD Ø36 +9 FDA UDI

Identifiers

Catalog Number
913-0709 FDA UDI
Primary DI / UDI-DI
03701037303528 FDA UDI
FDA Product Code
HSD FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

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

Category: Orthopaedic surgical procedure kit, non-medicated, reusable

Humelock II Cemented Reversible Shoulder by Fx Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fx Solutions

Sources (1)

  • FDA UDI 89d66e58-097d-4821-b19b-992415738685 34 fields · synced May 30, 2026