gudid
Primary ID: 901117
Welch Allyn, Inc. (UDI 901117)
Manufactured by WELCH ALLYN, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Welch Allyn, Inc. - Primary ID 901117
Device Regulatory Overview
The Welch Allyn, Inc. (Model/Catalog Number: 901117) is a medical device manufactured by WELCH ALLYN, INC.. This product is indexed under FDA Product Code / Category Classification FER within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 901117
- Product Code / EMDN
- FER
- Device Name
- LARGE OBTURATOR ASSY
- Database Sync Date
- 2026-08-09 09:54:37
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 Welch Allyn, Inc.?
The registered manufacturer of record for Welch Allyn, Inc. is WELCH ALLYN, INC..
What is the Primary UDI-DI identifier for Welch Allyn, Inc.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 901117.
What classification code is assigned to this device?
This device is registered under product classification code FER.
Similar Classification Devices (FER)
Other Devices by WELCH ALLYN, INC.
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