gudid
Primary ID: 1100-150LQ
Rochester Carmalt Forceps (UDI 1100-150LQ)
Manufactured by SONTEC INSTRUMENTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rochester Carmalt Forceps - Primary ID 1100-150LQ
Device Regulatory Overview
The Rochester Carmalt Forceps (Model/Catalog Number: 1100-150LQ) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification HTD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1100-150LQ
- Product Code / EMDN
- HTD
- Device Name
- Rochester Carmalt Forceps Longitudinal Cross Hatch Tip Straight Left Quantum
- Database Sync Date
- 2026-08-09 09:06:59
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 Rochester Carmalt Forceps?
The registered manufacturer of record for Rochester Carmalt Forceps is SONTEC INSTRUMENTS, INC..
What is the Primary UDI-DI identifier for Rochester Carmalt Forceps?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1100-150LQ.
What classification code is assigned to this device?
This device is registered under product classification code HTD.
Similar Classification Devices (HTD)
Other Devices by SONTEC INSTRUMENTS, INC.
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