Proscope™ (UDI 00634782035341)
Manufactured by American Diagnostic Corporation
Device Regulatory Overview
The Proscope™ (Model/Catalog Number: 5211) is a medical device manufactured by American Diagnostic Corporation. This product is indexed under FDA Product Code / Category Classification Z12040102,Z12120114,Z12149006 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5211
- Product Code / EMDN
- Z12040102,Z12120114,Z12149006
- Device Name
- Otoscope and parts
- Database Sync Date
- 2026-08-09 16:29:10
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 Proscope™?
The registered manufacturer of record for Proscope™ is American Diagnostic Corporation.
What is the Primary UDI-DI identifier for Proscope™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00634782035341.
What classification code is assigned to this device?
This device is registered under product classification code Z12040102,Z12120114,Z12149006.
Similar Classification Devices (Z12040102,Z12120114,Z12149006)
Other Devices by American Diagnostic Corporation
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