CAMPYLOBACTER SELECTIVE AGAR (SKIRROW) (UDI 05212037701453)
Manufactured by G. PAPANIKOLAOU & CO. LP - Bioprepare
Device Regulatory Overview
The CAMPYLOBACTER SELECTIVE AGAR (SKIRROW) (Model/Catalog Number: 010636) is a medical device manufactured by G. PAPANIKOLAOU & CO. LP - Bioprepare. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 010636
- Product Code / EMDN
- W0104010405
- Device Name
- CAMPYLOBACTER SELECTIVE AGAR (SKIRROW)
- Database Sync Date
- 2026-08-09 16:47:07
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 CAMPYLOBACTER SELECTIVE AGAR (SKIRROW)?
The registered manufacturer of record for CAMPYLOBACTER SELECTIVE AGAR (SKIRROW) is G. PAPANIKOLAOU & CO. LP - Bioprepare.
What is the Primary UDI-DI identifier for CAMPYLOBACTER SELECTIVE AGAR (SKIRROW)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05212037701453.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
Similar Classification Devices (W0104010405)
Other Devices by G. PAPANIKOLAOU & CO. LP - Bioprepare
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint