GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 06947752802619

Otoscope (UDI 06947752802619)

Manufactured by Tianjin Bolang Science-Technology Development Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Otoscope - Primary ID 06947752802619

Device Regulatory Overview

The Otoscope (Model/Catalog Number: ER33.140.WA) is a medical device manufactured by Tianjin Bolang Science-Technology Development Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification Z12149006 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ER33.140.WA
Product Code / EMDN
Z12149006
Device Name
Otoscope
Database Sync Date
2026-08-09 16:28:56

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 Otoscope?

The registered manufacturer of record for Otoscope is Tianjin Bolang Science-Technology Development Co.,Ltd..

What is the Primary UDI-DI identifier for Otoscope?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06947752802619.

What classification code is assigned to this device?

This device is registered under product classification code Z12149006.

Similar Classification Devices (Z12149006)

Other Devices by Tianjin Bolang Science-Technology Development Co.,Ltd.

Programmatic Export

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

JSON API Endpoint