FINGER SPLINT (UDI 06942272612335)
Manufactured by FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU)
Device Regulatory Overview
The FINGER SPLINT (Model/Catalog Number: 7cm*2.3cm) is a medical device manufactured by FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU). This product is indexed under FDA Product Code / Category Classification Y060603 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7cm*2.3cm
- Product Code / EMDN
- Y060603
- Device Name
- FINGER SPLINT
- Database Sync Date
- 2026-08-09 16:29:52
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of FINGER SPLINT?
The registered manufacturer of record for FINGER SPLINT is FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU).
What is the Primary UDI-DI identifier for FINGER SPLINT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942272612335.
What classification code is assigned to this device?
This device is registered under product classification code Y060603.
Similar Classification Devices (Y060603)
Other Devices by FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU)
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