GRAFT KIT - BONE AUGMENTATION INSTRUMENTS, BIONIK HANDLE (UDI 83-7101Z)
Manufactured by W.H. Holden, Inc.
Device Regulatory Overview
The GRAFT KIT - BONE AUGMENTATION INSTRUMENTS, BIONIK HANDLE (Model/Catalog Number: 83-7101Z) is a medical device manufactured by W.H. Holden, Inc.. This product is indexed under FDA Product Code / Category Classification DZN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 83-7101Z
- Product Code / EMDN
- DZN
- Device Name
- Database Sync Date
- 2026-08-09 09:01:13
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 GRAFT KIT - BONE AUGMENTATION INSTRUMENTS, BIONIK HANDLE?
The registered manufacturer of record for GRAFT KIT - BONE AUGMENTATION INSTRUMENTS, BIONIK HANDLE is W.H. Holden, Inc..
What is the Primary UDI-DI identifier for GRAFT KIT - BONE AUGMENTATION INSTRUMENTS, BIONIK HANDLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 83-7101Z.
What classification code is assigned to this device?
This device is registered under product classification code DZN.
Similar Classification Devices (DZN)
Other Devices by W.H. Holden, Inc.
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