Kitazato Blastomere Biopsy Micropipette (UDI MT-BPBM-20-30)
Manufactured by KITAZATO CORPORATION
Device Regulatory Overview
The Kitazato Blastomere Biopsy Micropipette (Model/Catalog Number: MT-BPBM-20-30) is a medical device manufactured by KITAZATO CORPORATION. This product is indexed under FDA Product Code / Category Classification PUC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MT-BPBM-20-30
- Product Code / EMDN
- PUC
- Device Name
- Database Sync Date
- 2026-08-09 09:15:37
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 Kitazato Blastomere Biopsy Micropipette?
The registered manufacturer of record for Kitazato Blastomere Biopsy Micropipette is KITAZATO CORPORATION.
What is the Primary UDI-DI identifier for Kitazato Blastomere Biopsy Micropipette?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MT-BPBM-20-30.
What classification code is assigned to this device?
This device is registered under product classification code PUC.
Similar Classification Devices (PUC)
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