Boject

GUDID 00382830042420

Bo-ject Needle

NATUS MANUFACTURING LIMITED

Electromyographic needle electrode, single-use Electromyographic needle electrode, single-use

• Primary Device ID: 00382830042420
• NIH Device Record Key: a83466a1-4004-45e7-a46e-75cd6d1964a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Boject
• Version Model Number: 9013S0422
• Company DUNS: 896421240
• Company Name: NATUS MANUFACTURING LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00382830042420 [Primary]

FDA Product Code

• IKT: Electrode, Needle, Diagnostic Electromyograph

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-06-11
• Device Publish Date: 2016-08-25

On-Brand Devices [Boject]

• 00382830042475: Bo-ject Needle
• 00382830042468: Bo-ject Needle
• 00382830042451: Bo-ject Needle
• 00382830042444: Bo-ject Needle
• 00382830042437: Bo-ject Needle
• 00382830042420: Bo-ject Needle