GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 08800016000368

BOMTECH (UDI 08800016000368)

Manufactured by BOMTECH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BOMTECH - Primary ID 08800016000368

Device Regulatory Overview

The BOMTECH (Model/Catalog Number: RF COMBO JECTOR) is a medical device manufactured by BOMTECH. This product is indexed under FDA Product Code / Category Classification Z12030302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RF COMBO JECTOR
Product Code / EMDN
Z12030302
Device Name
RF COMBO JECTOR
Database Sync Date
2026-08-09 17:01:47

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of BOMTECH?

The registered manufacturer of record for BOMTECH is BOMTECH.

What is the Primary UDI-DI identifier for BOMTECH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800016000368.

What classification code is assigned to this device?

This device is registered under product classification code Z12030302.

Similar Classification Devices (Z12030302)

Other Devices by BOMTECH

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint