gudid
Primary ID: BP019
BABY TISCHLER BIOPSY PUNCH 10" (UDI BP019)
Manufactured by BIOPSY FINE CUT INSTRUMENTS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BABY TISCHLER BIOPSY PUNCH 10" - Primary ID BP019
Device Regulatory Overview
The BABY TISCHLER BIOPSY PUNCH 10" (Model/Catalog Number: BP019) 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
- BP019
- Product Code / EMDN
- HFB
- Device Name
- Size 10"Made by Stainless Steel
- 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 BABY TISCHLER BIOPSY PUNCH 10"?
The registered manufacturer of record for BABY TISCHLER BIOPSY PUNCH 10" is BIOPSY FINE CUT INSTRUMENTS.
What is the Primary UDI-DI identifier for BABY TISCHLER BIOPSY PUNCH 10"?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BP019.
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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