eudamed_udi
Primary ID: 08904343712236
Appasamy (UDI 08904343712236)
Manufactured by Appasamy Associates Private Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Appasamy - Primary ID 08904343712236
Device Regulatory Overview
The Appasamy (Model/Catalog Number: AA 2210) is a medical device manufactured by Appasamy Associates Private Limited. This product is indexed under FDA Product Code / Category Classification L1715 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AA 2210
- Product Code / EMDN
- L1715
- Device Name
- SCLERAL MARKERS, REUSABLE
- Database Sync Date
- 2026-08-09 16:50:39
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 Appasamy?
The registered manufacturer of record for Appasamy is Appasamy Associates Private Limited.
What is the Primary UDI-DI identifier for Appasamy?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08904343712236.
What classification code is assigned to this device?
This device is registered under product classification code L1715.
Similar Classification Devices (L1715)
Other Devices by Appasamy Associates Private Limited
Programmatic Export
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