Rotor 24 place for capillaries 1023

GUDID 04050674030427

Hematocrit rotor, 24-place

Andreas Hettich GmbH & Co. KG

Microhaematocrit centrifuge

• Primary Device ID: 04050674030427
• NIH Device Record Key: d932172b-2808-4f20-8e72-cd43568b6ccb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rotor 24 place for capillaries
• Version Model Number: 1023
• Catalog Number: 1023
• Company DUNS: 316403245
• Company Name: Andreas Hettich GmbH & Co. KG
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	04050674030427 [Primary]

FDA Product Code

• JPI: Device, Hematocrit Measuring

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

On-Brand Devices [Rotor 24 place for capillaries]

• 04050674077675: Hematocrit rotor, 24-place
• 04050674030441: Hematocrit rotor, 24-place
• 04050674030427: Hematocrit rotor, 24-place
• 04050674030410: Hematocrit rotor, 24 place