gudid
Primary ID: DL300
HANK DILATOR DOUBLE ENDED 7/8 FR (UDI DL300)
Manufactured by BIOPSY FINE CUT INSTRUMENTS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HANK DILATOR DOUBLE ENDED 7/8 FR - Primary ID DL300
Device Regulatory Overview
The HANK DILATOR DOUBLE ENDED 7/8 FR (Model/Catalog Number: DL300) is a medical device manufactured by BIOPSY FINE CUT INSTRUMENTS. This product is indexed under FDA Product Code / Category Classification KCF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DL300
- Product Code / EMDN
- KCF
- Device Name
- HANK DILATOR DOUBLE ENDED 7/8 FR
- 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 HANK DILATOR DOUBLE ENDED 7/8 FR?
The registered manufacturer of record for HANK DILATOR DOUBLE ENDED 7/8 FR is BIOPSY FINE CUT INSTRUMENTS.
What is the Primary UDI-DI identifier for HANK DILATOR DOUBLE ENDED 7/8 FR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DL300.
What classification code is assigned to this device?
This device is registered under product classification code KCF.
Similar Classification Devices (KCF)
Other Devices by BIOPSY FINE CUT INSTRUMENTS
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