CARPAL GEL SLEEVE S1012 MIS. LXL DX - CONF. DA 1 PZ (UDI 08056598552256)
Manufactured by EUMEDICA SRL
Device Regulatory Overview
The CARPAL GEL SLEEVE S1012 MIS. LXL DX - CONF. DA 1 PZ (Model/Catalog Number: S1012LD) is a medical device manufactured by EUMEDICA SRL. This product is indexed under FDA Product Code / Category Classification M03030299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S1012LD
- Product Code / EMDN
- M03030299
- Device Name
- CICATRICI
- Database Sync Date
- 2026-08-09 16:47:03
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 CARPAL GEL SLEEVE S1012 MIS. LXL DX - CONF. DA 1 PZ?
The registered manufacturer of record for CARPAL GEL SLEEVE S1012 MIS. LXL DX - CONF. DA 1 PZ is EUMEDICA SRL.
What is the Primary UDI-DI identifier for CARPAL GEL SLEEVE S1012 MIS. LXL DX - CONF. DA 1 PZ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056598552256.
What classification code is assigned to this device?
This device is registered under product classification code M03030299.
Similar Classification Devices (M03030299)
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