ASSI (UDI ASSI.SP1015)
Manufactured by ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATION
Device Regulatory Overview
The ASSI (Model/Catalog Number: ASSI.SP1015) is a medical device manufactured by ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATION. This product is indexed under FDA Product Code / Category Classification KOH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ASSI.SP1015
- Product Code / EMDN
- KOH
- Device Name
- Silicone Operation Pad 11cmx15cm
- Database Sync Date
- 2026-08-09 09:39:15
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ASSI?
The registered manufacturer of record for ASSI is ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATION.
What is the Primary UDI-DI identifier for ASSI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ASSI.SP1015.
What classification code is assigned to this device?
This device is registered under product classification code KOH.
Similar Classification Devices (KOH)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint