Migele Gel Electrophoresis Unit 2118-0010

GUDID 06438147368907

Migele™ Gel Electrophoresis Unit (GEU) is intended for professional use together with power supply, water bath and isoelectric focusing (IEF) gels. GE

Wallac Oy

Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD, automated Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD Electrophoresis analyser IVD

• Primary Device ID: 06438147368907
• NIH Device Record Key: 0b42a432-a889-4ff1-9b4a-630a762d455c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Migele Gel Electrophoresis Unit
• Version Model Number: 2118-0010
• Catalog Number: 2118-0010
• Company DUNS: 540156544
• Company Name: Wallac Oy
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	06438147368907 [Primary]

FDA Product Code

• JJN: Apparatus, Electrophoresis, For Clinical Use

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-12-31
• Device Publish Date: 2018-11-28

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