“A-Spine” Orthopedic Manual Surgical Instruments (Non-Sterile) (UDI 04711021934040)
Manufactured by A-SPINE Asia Co., Ltd.
Device Regulatory Overview
The “A-Spine” Orthopedic Manual Surgical Instruments (Non-Sterile) (Model/Catalog Number: 229-1703) is a medical device manufactured by A-SPINE Asia Co., Ltd.. This product is indexed under FDA Product Code / Category Classification L0999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 229-1703
- Product Code / EMDN
- L0999
- Device Name
- Universal Insertor
- Database Sync Date
- 2026-08-09 16:28:48
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 “A-Spine” Orthopedic Manual Surgical Instruments (Non-Sterile)?
The registered manufacturer of record for “A-Spine” Orthopedic Manual Surgical Instruments (Non-Sterile) is A-SPINE Asia Co., Ltd..
What is the Primary UDI-DI identifier for “A-Spine” Orthopedic Manual Surgical Instruments (Non-Sterile)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04711021934040.
What classification code is assigned to this device?
This device is registered under product classification code L0999.
Similar Classification Devices (L0999)
Other Devices by A-SPINE Asia Co., Ltd.
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