gudid
Primary ID: LZ108
Lletz TENACULUM FORCEPS 9.5" (UDI LZ108)
Manufactured by BIOPSY FINE CUT INSTRUMENTS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lletz TENACULUM FORCEPS 9.5" - Primary ID LZ108
Device Regulatory Overview
The Lletz TENACULUM FORCEPS 9.5" (Model/Catalog Number: LZ108) is a medical device manufactured by BIOPSY FINE CUT INSTRUMENTS. This product is indexed under FDA Product Code / Category Classification HTD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LZ108
- Product Code / EMDN
- HTD
- Device Name
- Lletz TENACULUM FORCEPS 9.5"
- Database Sync Date
- 2026-08-09 09:03:52
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 Lletz TENACULUM FORCEPS 9.5"?
The registered manufacturer of record for Lletz TENACULUM FORCEPS 9.5" is BIOPSY FINE CUT INSTRUMENTS.
What is the Primary UDI-DI identifier for Lletz TENACULUM FORCEPS 9.5"?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LZ108.
What classification code is assigned to this device?
This device is registered under product classification code HTD.
Similar Classification Devices (HTD)
Other Devices by BIOPSY FINE CUT INSTRUMENTS
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