gudid
Primary ID: 83-2004
REZNICK MEMBRANE HOLDING FORCEPS (UDI 83-2004)
Manufactured by W.H. Holden, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for REZNICK MEMBRANE HOLDING FORCEPS - Primary ID 83-2004
Device Regulatory Overview
The REZNICK MEMBRANE HOLDING FORCEPS (Model/Catalog Number: 83-2004) is a medical device manufactured by W.H. Holden, Inc.. This product is indexed under FDA Product Code / Category Classification HTD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 83-2004
- Product Code / EMDN
- HTD
- 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 REZNICK MEMBRANE HOLDING FORCEPS?
The registered manufacturer of record for REZNICK MEMBRANE HOLDING FORCEPS is W.H. Holden, Inc..
What is the Primary UDI-DI identifier for REZNICK MEMBRANE HOLDING FORCEPS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 83-2004.
What classification code is assigned to this device?
This device is registered under product classification code HTD.
Similar Classification Devices (HTD)
Other Devices by W.H. Holden, Inc.
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