GUDIDData
eudamed_udi Primary ID: 06931038600303

diagnostic hammer (UDI 06931038600303)

Manufactured by Wenzhou Bokang Instruments Co.,Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for diagnostic hammer - Primary ID 06931038600303

Device Regulatory Overview

The diagnostic hammer (Model/Catalog Number: BK5503) is a medical device manufactured by Wenzhou Bokang Instruments Co.,Ltd. This product is indexed under FDA Product Code / Category Classification L160199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BK5503
Product Code / EMDN
L160199
Device Name
diagnostic hammer
Database Sync Date
2026-08-09 18:34:15

Full Regulatory Attributes

πŸ”’ Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of diagnostic hammer?

The registered manufacturer of record for diagnostic hammer is Wenzhou Bokang Instruments Co.,Ltd.

What is the Primary UDI-DI identifier for diagnostic hammer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06931038600303.

What classification code is assigned to this device?

This device is registered under product classification code L160199.

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