CHROMART CRE SUPPLEMENT - 10 fl (1x500 mL T) (UDI 08056450503624)
Manufactured by Biolife Italiana s.r.l.
Device Regulatory Overview
The CHROMART CRE SUPPLEMENT - 10 fl (1x500 mL T) (Model/Catalog Number: 4240082) is a medical device manufactured by Biolife Italiana s.r.l.. This product is indexed under FDA Product Code / Category Classification W0104010104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4240082
- Product Code / EMDN
- W0104010104
- Device Name
- ADDITIVES FOR CULTURE MEDIA
- Database Sync Date
- 2026-08-09 17:04:28
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of CHROMART CRE SUPPLEMENT - 10 fl (1x500 mL T)?
The registered manufacturer of record for CHROMART CRE SUPPLEMENT - 10 fl (1x500 mL T) is Biolife Italiana s.r.l..
What is the Primary UDI-DI identifier for CHROMART CRE SUPPLEMENT - 10 fl (1x500 mL T)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056450503624.
What classification code is assigned to this device?
This device is registered under product classification code W0104010104.
Similar Classification Devices (W0104010104)
Other Devices by Biolife Italiana s.r.l.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint