eudamed_udi
Primary ID: B961DDPD35380
EXCAVATORS SPOON 17 SPOON (UDI B961DDPD35380)
Manufactured by Daddy D Pro
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EXCAVATORS SPOON 17 SPOON - Primary ID B961DDPD35380
Device Regulatory Overview
The EXCAVATORS SPOON 17 SPOON (Model/Catalog Number: DDP-D3-538) is a medical device manufactured by Daddy D Pro. This product is indexed under FDA Product Code / Category Classification L159002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DDP-D3-538
- Product Code / EMDN
- L159002
- Device Name
- EXCAVATORS SPOON 17 SPOON
- Database Sync Date
- 2026-08-09 16:28:48
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 EXCAVATORS SPOON 17 SPOON?
The registered manufacturer of record for EXCAVATORS SPOON 17 SPOON is Daddy D Pro.
What is the Primary UDI-DI identifier for EXCAVATORS SPOON 17 SPOON?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B961DDPD35380.
What classification code is assigned to this device?
This device is registered under product classification code L159002.
Similar Classification Devices (L159002)
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