Unspecified Brand (UDI 04250381803639)
Manufactured by SPIGGLE & THEIS Medizintechnik GmbH
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 11000-D30) is a medical device manufactured by SPIGGLE & THEIS Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification P020180 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11000-D30
- Product Code / EMDN
- P020180
- Device Name
- Dummy length sizer for middle ear implants
- Database Sync Date
- 2026-08-09 16:49:53
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is SPIGGLE & THEIS Medizintechnik GmbH.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250381803639.
What classification code is assigned to this device?
This device is registered under product classification code P020180.
Similar Classification Devices (P020180)
Other Devices by SPIGGLE & THEIS Medizintechnik GmbH
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