eudamed_udi
Primary ID: 00850023741455
CER-ORTHO (UDI 00850023741455)
Manufactured by Ranfac Corp.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CER-ORTHO - Primary ID 00850023741455
Device Regulatory Overview
The CER-ORTHO (Model/Catalog Number: 74396-01M) is a medical device manufactured by Ranfac Corp.. This product is indexed under FDA Product Code / Category Classification A01020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 74396-01M
- Product Code / EMDN
- A01020102
- Device Name
- Ranfac Bone Marrow Aspiration Needle
- Database Sync Date
- 2026-08-09 16:29:35
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 CER-ORTHO?
The registered manufacturer of record for CER-ORTHO is Ranfac Corp..
What is the Primary UDI-DI identifier for CER-ORTHO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00850023741455.
What classification code is assigned to this device?
This device is registered under product classification code A01020102.
Similar Classification Devices (A01020102)
Other Devices by Ranfac Corp.
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