Embra® Nonwoven swabs 10 x 10 cm, 5-pack, sterile (UDI 06438129170443)
Manufactured by OneMed Group Oy
Device Regulatory Overview
The Embra® Nonwoven swabs 10 x 10 cm, 5-pack, sterile (Model/Catalog Number: 223274503) is a medical device manufactured by OneMed Group Oy. This product is indexed under FDA Product Code / Category Classification M0202010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 223274503
- Product Code / EMDN
- M0202010101
- Device Name
- Swabs Nonwoven, folded, sterile
- Database Sync Date
- 2026-08-09 16:29:38
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 Embra® Nonwoven swabs 10 x 10 cm, 5-pack, sterile?
The registered manufacturer of record for Embra® Nonwoven swabs 10 x 10 cm, 5-pack, sterile is OneMed Group Oy.
What is the Primary UDI-DI identifier for Embra® Nonwoven swabs 10 x 10 cm, 5-pack, sterile?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438129170443.
What classification code is assigned to this device?
This device is registered under product classification code M0202010101.
Similar Classification Devices (M0202010101)
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