gudid
Primary ID: BCNHTSUTS32
Harris Teeter (UDI BCNHTSUTS32)
Manufactured by AL-BAD MASSUOT YITZHAK LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Harris Teeter - Primary ID BCNHTSUTS32
Device Regulatory Overview
The Harris Teeter (Model/Catalog Number: BCNHTSUTS32) is a medical device manufactured by AL-BAD MASSUOT YITZHAK LTD. This product is indexed under FDA Product Code / Category Classification HHD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BCNHTSUTS32
- Product Code / EMDN
- HHD
- Device Name
- Database Sync Date
- 2026-08-09 09:08:47
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 Harris Teeter?
The registered manufacturer of record for Harris Teeter is AL-BAD MASSUOT YITZHAK LTD.
What is the Primary UDI-DI identifier for Harris Teeter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BCNHTSUTS32.
What classification code is assigned to this device?
This device is registered under product classification code HHD.
Similar Classification Devices (HHD)
Other Devices by AL-BAD MASSUOT YITZHAK LTD
Programmatic Export
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