eudamed_udi
Primary ID: 15060069282610
Acute IV Plus (UDI 15060069282610)
Manufactured by Richardson Healthcare Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Acute IV Plus - Primary ID 15060069282610
Device Regulatory Overview
The Acute IV Plus (Model/Catalog Number: 908080) is a medical device manufactured by Richardson Healthcare Limited. This product is indexed under FDA Product Code / Category Classification T0203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 908080
- Product Code / EMDN
- T0203
- Device Name
- Acute IV Plus Acute Cannulation Pack, 1 blister per pack, 60 packs per case
- Database Sync Date
- 2026-08-09 16:45:51
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 Acute IV Plus?
The registered manufacturer of record for Acute IV Plus is Richardson Healthcare Limited.
What is the Primary UDI-DI identifier for Acute IV Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15060069282610.
What classification code is assigned to this device?
This device is registered under product classification code T0203.
Similar Classification Devices (T0203)
Other Devices by Richardson Healthcare Limited
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