VACUSERA (UDI +M712238400A1F)
Manufactured by DİSERA TIBBİ MALZEME LOJİSTİK SAN. VE TİC. A.Ş.
Device Regulatory Overview
The VACUSERA (Model/Catalog Number: 238400A) is a medical device manufactured by DİSERA TIBBİ MALZEME LOJİSTİK SAN. VE TİC. A.Ş.. This product is indexed under FDA Product Code / Category Classification B010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 238400A
- Product Code / EMDN
- B010202
- Device Name
- VACUSERA Biostimulants Exera
- Database Sync Date
- 2026-08-09 16:29:15
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 VACUSERA?
The registered manufacturer of record for VACUSERA is DİSERA TIBBİ MALZEME LOJİSTİK SAN. VE TİC. A.Ş..
What is the Primary UDI-DI identifier for VACUSERA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +M712238400A1F.
What classification code is assigned to this device?
This device is registered under product classification code B010202.
Similar Classification Devices (B010202)
Other Devices by DİSERA TIBBİ MALZEME LOJİSTİK SAN. VE TİC. A.Ş.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint