gudid
Primary ID: SP96-8322
Snowden-Pencer (UDI SP96-8322)
Manufactured by CAREFUSION 2200, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Snowden-Pencer - Primary ID SP96-8322
Device Regulatory Overview
The Snowden-Pencer (Model/Catalog Number: SP96-8322) is a medical device manufactured by CAREFUSION 2200, INC. This product is indexed under FDA Product Code / Category Classification GCJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SP96-8322
- Product Code / EMDN
- GCJ
- Device Name
- Snowden-Pencer MIS ERGONOMIC TAKE-APART IN-LINE LONG JAW NEEDLE HOLDER ROTATING, RATCHETED HANDLE 5MM, 36CM, COMPLETE INSTRUMENT
- Database Sync Date
- 2026-08-09 09:16:32
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 Snowden-Pencer?
The registered manufacturer of record for Snowden-Pencer is CAREFUSION 2200, INC.
What is the Primary UDI-DI identifier for Snowden-Pencer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SP96-8322.
What classification code is assigned to this device?
This device is registered under product classification code GCJ.
Similar Classification Devices (GCJ)
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