eudamed_udi
Primary ID: 08715343056783
Kliniplast (UDI 08715343056783)
Manufactured by Aso Philippines, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kliniplast - Primary ID 08715343056783
Device Regulatory Overview
The Kliniplast (Model/Catalog Number: MED-4294121) is a medical device manufactured by Aso Philippines, Inc.. This product is indexed under FDA Product Code / Category Classification M0599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MED-4294121
- Product Code / EMDN
- M0599
- Device Name
- Blue detectable adhesive bandages
- Database Sync Date
- 2026-08-09 16:29:23
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 Kliniplast?
The registered manufacturer of record for Kliniplast is Aso Philippines, Inc..
What is the Primary UDI-DI identifier for Kliniplast?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08715343056783.
What classification code is assigned to this device?
This device is registered under product classification code M0599.
Similar Classification Devices (M0599)
Other Devices by Aso Philippines, Inc.
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