eudamed_udi
Primary ID: 00840682142748
Lullaby Resus Plus – NIST (UDI 00840682142748)
Manufactured by Datex-Ohmeda Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lullaby Resus Plus – NIST - Primary ID 00840682142748
Device Regulatory Overview
The Lullaby Resus Plus – NIST (Model/Catalog Number: 2070100-001) is a medical device manufactured by Datex-Ohmeda Inc.. This product is indexed under FDA Product Code / Category Classification Z12080499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2070100-001
- Product Code / EMDN
- Z12080499
- Device Name
- Lullaby Resus Plus
- Database Sync Date
- 2026-08-09 16:29:27
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 Lullaby Resus Plus – NIST?
The registered manufacturer of record for Lullaby Resus Plus – NIST is Datex-Ohmeda Inc..
What is the Primary UDI-DI identifier for Lullaby Resus Plus – NIST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840682142748.
What classification code is assigned to this device?
This device is registered under product classification code Z12080499.
Similar Classification Devices (Z12080499)
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