eudamed_udi
Primary ID: 08907265012668
PM-O-LINE (UDI 08907265012668)
Manufactured by Romsons Group Private Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PM-O-LINE - Primary ID 08907265012668
Device Regulatory Overview
The PM-O-LINE (Model/Catalog Number: GS-3036 KAD) is a medical device manufactured by Romsons Group Private Limited. This product is indexed under FDA Product Code / Category Classification A03020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GS-3036 KAD
- Product Code / EMDN
- A03020102
- Device Name
- EXTENSION LINES
- Database Sync Date
- 2026-08-09 16:29:07
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 PM-O-LINE?
The registered manufacturer of record for PM-O-LINE is Romsons Group Private Limited.
What is the Primary UDI-DI identifier for PM-O-LINE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08907265012668.
What classification code is assigned to this device?
This device is registered under product classification code A03020102.
Similar Classification Devices (A03020102)
Other Devices by Romsons Group Private Limited
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