Reference instrument (UDI 10-654-50)
Manufactured by Spiggle & Theis Medizintechnik GmbH
Device Regulatory Overview
The Reference instrument (Model/Catalog Number: 10-654-50) is a medical device manufactured by Spiggle & Theis Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification JYJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-654-50
- Product Code / EMDN
- JYJ
- Device Name
- for middle ear prostheses length 5.0 mm, 16 cm
- Database Sync Date
- 2026-08-09 09:11:39
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 Reference instrument?
The registered manufacturer of record for Reference instrument is Spiggle & Theis Medizintechnik GmbH.
What is the Primary UDI-DI identifier for Reference instrument?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-654-50.
What classification code is assigned to this device?
This device is registered under product classification code JYJ.
Similar Classification Devices (JYJ)
Other Devices by Spiggle & Theis Medizintechnik GmbH
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