Medtronic 2696 Patient Assistant ID Label
Label Dimensions and Markings
The label has a width of 1.770 inches and a height of 1.195 inches. It features the following markings:
- Model Name: Model 2696 InCheck™ Patient Assistant
- Regulatory Markings:
- [Person symbol]
- CE 0123
- [UL symbol]
- [CSA symbol]
- Country of Origin: USA Ronly
- Regulatory Compliance: UL2601-1 CAN/CSA C22.2 NO.601.1
- FCC ID: LF52696
- Manufacturer: Medtronic, Inc., Minneapolis, MN, USA
- Part Number: 4827-100
Technical Notes
- Material: 10 mil polycarbonate with velvet/matte texture. Adhesive: 3M 467MP, 2 mil.
-
Environmental Conditions/Testing:
- Operating Temperature Range: 0° to 125°F.
- Storage Temperature Range: -40° to 150°F.
- Thermal Shock: 150°F to room temperature, room temperature to -40°F (3 cycles).
- Humidity: 95% @ 95°F for 21 days.
- ESD: Maximum air gap discharge 20kV.
- Chemical Resistance: Resistant to water, alcohol (methyl, ethyl and isopropyl) and mild detergent.
-
Colors:
- Background: Medtronic Medium Gray, P/N 186034-001.
- Text & Symbols: Medtronic Dark Blue, P/N 186031-001.
- Artwork shown for reference only; refer to electronic version.
- Bold items indicate Plexus inspection requirements.
Manufacturing Information
This label is part of the main production for Plexus Technology Group. The drawing is designated as CONFIDENTIAL and contains proprietary information.
Drawing Details:
- Scale: 2:1
- Dimensions in Inches
- Tolerances: Linear X, X ± 0.1; X.XX ± 0.02; X.XXX ± 0.010; Angles ±0.5°
- Revision Date: March 4, 2003
- Part Number: 4827-100
- Sheet: 1 of 1
Related Documents
![]() |
Руководство оператора монитора пациента Medtronic INVOS™ Подробное руководство оператора для монитора пациента Medtronic INVOS™. Охватывает установку, эксплуатацию, обслуживание, устранение неисправностей и технические характеристики устройства. |
![]() |
Medtronic InterStim MRI Guidelines: Ensuring Patient Safety Comprehensive guidelines for conducting MRI scans on patients with Medtronic InterStim neurostimulation systems. Covers eligibility, equipment, scan conditions, and safety precautions for both full-body and head-only scans. |
![]() |
Medtronic 97740 : Manuel d'utilisation de la télécommande patient pour neurostimulation Guide d'utilisation complet de la télécommande patient Medtronic modèle 97740, conçue pour les systèmes de neurostimulation utilisés dans le traitement de la douleur. Ce manuel fournit des instructions détaillées sur le fonctionnement, la personnalisation de la thérapie, la maintenance et les précautions de sécurité. |
![]() |
Medtronic LINQ II Insertable Cardiac Monitor Clinician Manual Medtronic LINQ II Insertable Cardiac Monitor (ICM) Clinician Manual (Model LNQ22). This guide details the insertion, operation, monitoring, and technical specifications of the LINQ II ICM, a device for continuous cardiac monitoring and arrhythmia detection. It covers system components, clinical applications, data management via the CareLink Network, and troubleshooting for healthcare professionals. |
![]() |
Medtronic InterStim Systems MRI Guidelines Comprehensive guidelines for performing Magnetic Resonance Imaging (MRI) scans on patients with Medtronic InterStim neurostimulation systems. This document details MR Conditional status, potential risks, eligibility determination, and procedural steps for both full-body and head-only MRI scans. |
![]() |
Medtronic MyCareLink Smart Patient Monitor: Android & iOS Basics Guide This guide explains how to use the Medtronic MyCareLink Smart Patient Monitor with Android and iOS devices. It covers app installation, Wi-Fi/Bluetooth setup, compatibility, and troubleshooting. Note: All patient data shown is for demonstration purposes only. |
![]() |
Medtronic DBS Therapy Patient Programmer Quick Guide A quick guide for using the Medtronic DBS Therapy Patient Programmer, Model TH90, for Activa devices. Learn how to view therapy, check battery status, change groups, and adjust stimulation. |
![]() |
MyCareLink Smart Patient Monitor Troubleshooting Guide This guide provides troubleshooting steps for common system messages encountered with the MyCareLink Smart Patient Monitor. It covers issues related to batteries, Wi-Fi/cellular connections, data transmission, Bluetooth, and software updates. |