GUDIDData
eudamed_udi Primary ID: 00853508002348

BE-ST NIM Pedicle Probe (UDI 00853508002348)

Manufactured by Lacey Manufacturing Company LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BE-ST NIM Pedicle Probe - Primary ID 00853508002348

Device Regulatory Overview

The BE-ST NIM Pedicle Probe (Model/Catalog Number: PK1013) is a medical device manufactured by Lacey Manufacturing Company LLC. This product is indexed under FDA Product Code / Category Classification A0399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PK1013
Product Code / EMDN
A0399
Device Name
NIM Pedicle Probe Thoracic
Database Sync Date
2026-08-09 16:47:19

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of BE-ST NIM Pedicle Probe?

The registered manufacturer of record for BE-ST NIM Pedicle Probe is Lacey Manufacturing Company LLC.

What is the Primary UDI-DI identifier for BE-ST NIM Pedicle Probe?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00853508002348.

What classification code is assigned to this device?

This device is registered under product classification code A0399.

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