Unspecified Brand (UDI 08961101443221)
Manufactured by Towne Brothers (Private) Limited
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 101-112-2-H) is a medical device manufactured by Towne Brothers (Private) Limited. This product is indexed under FDA Product Code / Category Classification L159013 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 101-112-2-H
- Product Code / EMDN
- L159013
- Device Name
- Cement Spatula No. 2 D/Ended , SS.(hollow handle)
- Database Sync Date
- 2026-08-09 16:29:24
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Towne Brothers (Private) Limited.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08961101443221.
What classification code is assigned to this device?
This device is registered under product classification code L159013.
Similar Classification Devices (L159013)
Other Devices by Towne Brothers (Private) Limited
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint