gudid
Primary ID: 40-0100HF
PERIO KNIFE GOLDMAN FOX 7 HF HANDLE (UDI 40-0100HF)
Manufactured by W.H. Holden, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PERIO KNIFE GOLDMAN FOX 7 HF HANDLE - Primary ID 40-0100HF
Device Regulatory Overview
The PERIO KNIFE GOLDMAN FOX 7 HF HANDLE (Model/Catalog Number: 40-0100HF) is a medical device manufactured by W.H. Holden, Inc.. This product is indexed under FDA Product Code / Category Classification EMO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 40-0100HF
- Product Code / EMDN
- EMO
- Device Name
- Database Sync Date
- 2026-08-09 09:01:14
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 PERIO KNIFE GOLDMAN FOX 7 HF HANDLE?
The registered manufacturer of record for PERIO KNIFE GOLDMAN FOX 7 HF HANDLE is W.H. Holden, Inc..
What is the Primary UDI-DI identifier for PERIO KNIFE GOLDMAN FOX 7 HF HANDLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 40-0100HF.
What classification code is assigned to this device?
This device is registered under product classification code EMO.
Similar Classification Devices (EMO)
Other Devices by W.H. Holden, Inc.
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