eudamed_udi
Primary ID: 00887761984189
Liftsheet Octo (UDI 00887761984189)
Manufactured by Liko Aktiebolag
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Liftsheet Octo - Primary ID 00887761984189
Device Regulatory Overview
The Liftsheet Octo (Model/Catalog Number: 3683105) is a medical device manufactured by Liko Aktiebolag. This product is indexed under FDA Product Code / Category Classification V0805038001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3683105
- Product Code / EMDN
- V0805038001
- Device Name
- Non-rigid body-support unit
- Database Sync Date
- 2026-08-09 17:08:16
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 Liftsheet Octo?
The registered manufacturer of record for Liftsheet Octo is Liko Aktiebolag.
What is the Primary UDI-DI identifier for Liftsheet Octo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00887761984189.
What classification code is assigned to this device?
This device is registered under product classification code V0805038001.
Similar Classification Devices (V0805038001)
Other Devices by Liko Aktiebolag
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