eudamed_udi
Primary ID: 06974567463414
Obliž (UDI 06974567463414)
Manufactured by Danyang Sunmed Healthcare Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Obliž - Primary ID 06974567463414
Device Regulatory Overview
The Obliž (Model/Catalog Number: -) is a medical device manufactured by Danyang Sunmed Healthcare Corporation. This product is indexed under FDA Product Code / Category Classification H900299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- -
- Product Code / EMDN
- H900299
- Device Name
- surgical tape
- Database Sync Date
- 2026-08-09 16:29:00
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 Obliž?
The registered manufacturer of record for Obliž is Danyang Sunmed Healthcare Corporation.
What is the Primary UDI-DI identifier for Obliž?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974567463414.
What classification code is assigned to this device?
This device is registered under product classification code H900299.
Similar Classification Devices (H900299)
Other Devices by Danyang Sunmed Healthcare Corporation
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