gudid
Primary ID: 21005
STERRAD (UDI 21005)
Manufactured by ADVANCED STERILIZATION PRODUCTS SERVICES INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STERRAD - Primary ID 21005
Device Regulatory Overview
The STERRAD (Model/Catalog Number: 21005) is a medical device manufactured by ADVANCED STERILIZATION PRODUCTS SERVICES INC.. This product is indexed under FDA Product Code / Category Classification JTQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 21005
- Product Code / EMDN
- JTQ
- Device Name
- Incubator 120V 58 C
- Database Sync Date
- 2026-08-09 10:00:20
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 STERRAD?
The registered manufacturer of record for STERRAD is ADVANCED STERILIZATION PRODUCTS SERVICES INC..
What is the Primary UDI-DI identifier for STERRAD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 21005.
What classification code is assigned to this device?
This device is registered under product classification code JTQ.
Similar Classification Devices (JTQ)
Other Devices by ADVANCED STERILIZATION PRODUCTS SERVICES INC.
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