Para 12 Extend 218994

GUDID 30844509000632

A Multi-Parameter Assayed Hematology Control for Instruments Offering a 3-Part Differential. Contains 6 vials of high level.

STRECK, INC.

Full blood count IVD, control

• Primary Device ID: 30844509000632
• NIH Device Record Key: 0ee54399-535c-46b0-94b2-3642df6ab06a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Para 12 Extend
• Version Model Number: 218994
• Catalog Number: 218994
• Company DUNS: 072915986
• Company Name: STRECK, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: false

Customer Support Contacts

• Phone: 1-800-228-6090
• Email: custserv@streck.com
• Phone: 1-800-228-6090
• Email: custserv@streck.com

Device Dimensions

• Total Volume: 2.5 Milliliter
• Total Volume: 2.5 Milliliter

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 10 Degrees Celsius
• Storage Environment Temperature: Between 2 Degrees Celsius and 10 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	30844509000632 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K823498

FDA Product Code

• GLQ: Mixture, Control, White-Cell And Red-Cell Indices

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-14

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