gudid
Primary ID: WP-881
OTOCELL Instrument Wipe (UDI WP-881)
Manufactured by Boston Medical Products, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OTOCELL Instrument Wipe - Primary ID WP-881
Device Regulatory Overview
The OTOCELL Instrument Wipe (Model/Catalog Number: WP-881) is a medical device manufactured by Boston Medical Products, Inc.. This product is indexed under FDA Product Code / Category Classification NAB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WP-881
- Product Code / EMDN
- NAB
- Device Name
- Size: 0.1 x 8.25 x 8.25 cm
- Database Sync Date
- 2026-08-09 09:23:54
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 OTOCELL Instrument Wipe?
The registered manufacturer of record for OTOCELL Instrument Wipe is Boston Medical Products, Inc..
What is the Primary UDI-DI identifier for OTOCELL Instrument Wipe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is WP-881.
What classification code is assigned to this device?
This device is registered under product classification code NAB.
Similar Classification Devices (NAB)
Other Devices by Boston Medical Products, Inc.
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