THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope (UDI Truncated Anoscope Medium Sterile)
Manufactured by THD SPA
Device Regulatory Overview
The THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope (Model/Catalog Number: Truncated Anoscope Medium Sterile) is a medical device manufactured by THD SPA. This product is indexed under FDA Product Code / Category Classification GCP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Truncated Anoscope Medium Sterile
- Product Code / EMDN
- GCP
- Device Name
- The THD anoscope is a disposable medical device deemed for investigation of the anal canal.Available with truncated or beveled tip.
- Database Sync Date
- 2026-08-09 09:04:34
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 THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope?
The registered manufacturer of record for THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope is THD SPA.
What is the Primary UDI-DI identifier for THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Truncated Anoscope Medium Sterile.
What classification code is assigned to this device?
This device is registered under product classification code GCP.
Similar Classification Devices (GCP)
Other Devices by THD SPA
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