gudid
Primary ID: FD-210U
DISPOSABLE HOT BIOPSY FORCEPS (UDI FD-210U)
Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DISPOSABLE HOT BIOPSY FORCEPS - Primary ID FD-210U
Device Regulatory Overview
The DISPOSABLE HOT BIOPSY FORCEPS (Model/Catalog Number: FD-210U) is a medical device manufactured by OLYMPUS MEDICAL SYSTEMS CORP.. This product is indexed under FDA Product Code / Category Classification KGE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FD-210U
- Product Code / EMDN
- KGE
- Device Name
- DISPOSABLE HOT BIOPSY FORCEPS
- Database Sync Date
- 2026-08-09 09:46:01
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 DISPOSABLE HOT BIOPSY FORCEPS?
The registered manufacturer of record for DISPOSABLE HOT BIOPSY FORCEPS is OLYMPUS MEDICAL SYSTEMS CORP..
What is the Primary UDI-DI identifier for DISPOSABLE HOT BIOPSY FORCEPS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FD-210U.
What classification code is assigned to this device?
This device is registered under product classification code KGE.
Similar Classification Devices (KGE)
Other Devices by OLYMPUS MEDICAL SYSTEMS CORP.
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