gudid
Primary ID: FC006
INSTRUMENT F. REMOVAL OF I.U.D (UDI FC006)
Manufactured by BIOPSY FINE CUT INSTRUMENTS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INSTRUMENT F. REMOVAL OF I.U.D - Primary ID FC006
Device Regulatory Overview
The INSTRUMENT F. REMOVAL OF I.U.D (Model/Catalog Number: FC006) is a medical device manufactured by BIOPSY FINE CUT INSTRUMENTS. This product is indexed under FDA Product Code / Category Classification ELA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FC006
- Product Code / EMDN
- ELA
- Device Name
- INSTRUMENT F. REMOVAL OF I.U.D 12"
- 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 INSTRUMENT F. REMOVAL OF I.U.D?
The registered manufacturer of record for INSTRUMENT F. REMOVAL OF I.U.D is BIOPSY FINE CUT INSTRUMENTS.
What is the Primary UDI-DI identifier for INSTRUMENT F. REMOVAL OF I.U.D?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FC006.
What classification code is assigned to this device?
This device is registered under product classification code ELA.
Similar Classification Devices (ELA)
Other Devices by BIOPSY FINE CUT INSTRUMENTS
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