COLOSTOMY BAGS FOR TWO-PART SYSTEMS, W/O TISSUE COVER (UDI A10020201)
Device Regulatory Overview
The COLOSTOMY BAGS FOR TWO-PART SYSTEMS, W/O TISSUE COVER (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification A10020201 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous Cardiac Ablation Catheter...
FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, I...
SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System...
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- A10020201
- Device Name
- COLOSTOMY BAGS FOR TWO-PART SYSTEMS, W/O TISSUE COVER
- Database Sync Date
- 2026-08-09 16:18:37
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 COLOSTOMY BAGS FOR TWO-PART SYSTEMS, W/O TISSUE COVER?
The registered manufacturer of record for COLOSTOMY BAGS FOR TWO-PART SYSTEMS, W/O TISSUE COVER is .
What is the Primary UDI-DI identifier for COLOSTOMY BAGS FOR TWO-PART SYSTEMS, W/O TISSUE COVER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A10020201.
What classification code is assigned to this device?
This device is registered under product classification code A10020201.
Similar Classification Devices (A10020201)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint