gudid
Primary ID: SP104
PEDERSON SPECULUM MEDIUM (UDI SP104)
Manufactured by BIOPSY FINE CUT INSTRUMENTS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PEDERSON SPECULUM MEDIUM - Primary ID SP104
Device Regulatory Overview
The PEDERSON SPECULUM MEDIUM (Model/Catalog Number: SP104) is a medical device manufactured by BIOPSY FINE CUT INSTRUMENTS. This product is indexed under FDA Product Code / Category Classification HDF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SP104
- Product Code / EMDN
- HDF
- Device Name
- PEDERSON SPECULUM MEDIUM
- Database Sync Date
- 2026-08-09 09:03:52
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 PEDERSON SPECULUM MEDIUM?
The registered manufacturer of record for PEDERSON SPECULUM MEDIUM is BIOPSY FINE CUT INSTRUMENTS.
What is the Primary UDI-DI identifier for PEDERSON SPECULUM MEDIUM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SP104.
What classification code is assigned to this device?
This device is registered under product classification code HDF.
Similar Classification Devices (HDF)
Other Devices by BIOPSY FINE CUT INSTRUMENTS
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