gudid
Primary ID: BP109
ROTO TISCHLER BIOPSY PUNCH 10" (UDI BP109)
Manufactured by BIOPSY FINE CUT INSTRUMENTS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ROTO TISCHLER BIOPSY PUNCH 10" - Primary ID BP109
Device Regulatory Overview
The ROTO TISCHLER BIOPSY PUNCH 10" (Model/Catalog Number: BP109) is a medical device manufactured by BIOPSY FINE CUT INSTRUMENTS. This product is indexed under FDA Product Code / Category Classification HFB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BP109
- Product Code / EMDN
- HFB
- Device Name
- ROTO TISCHLER BIOPSY PUNCH 10" UP, COMPLETE SET HANDLE+TIP
- Database Sync Date
- 2026-08-09 09:03:52
Full Regulatory Attributes
🔒 Token Gated
{
"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 ROTO TISCHLER BIOPSY PUNCH 10"?
The registered manufacturer of record for ROTO TISCHLER BIOPSY PUNCH 10" is BIOPSY FINE CUT INSTRUMENTS.
What is the Primary UDI-DI identifier for ROTO TISCHLER BIOPSY PUNCH 10"?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BP109.
What classification code is assigned to this device?
This device is registered under product classification code HFB.
Similar Classification Devices (HFB)
Other Devices by BIOPSY FINE CUT INSTRUMENTS
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