SFG Micropipettor

GUDID 10850068289544

SPECTRUM FERTILITY GROUP INC.

Mechanical pipette

• Primary Device ID: 10850068289544
• NIH Device Record Key: 995b8365-6f28-4887-8a6b-abd10470cde4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SFG Micropipettor
• Version Model Number: S-MP-BK
• Company DUNS: 119292307
• Company Name: SPECTRUM FERTILITY GROUP INC.
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10850068289544 [Primary]

FDA Product Code

• MQJ: Micromanipulators And Microinjectors, Assisted Reproduction

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: 2024-11-20
• Device Publish Date: 2024-11-12

Devices Manufactured by SPECTRUM FERTILITY GROUP INC.

• 00850068289004 - SFG Denuding pipettes: 2024-11-20
• 00850068289011 - SFG Denuding pipettes: 2024-11-20
• 00850068289028 - SFG Denuding pipettes: 2024-11-20
• 00850068289035 - SFG Denuding pipettes: 2024-11-20
• 00850068289042 - SFG Denuding pipettes: 2024-11-20
• 00850068289059 - SFG Denuding pipettes: 2024-11-20
• 00850068289066 - SFG Denuding pipettes: 2024-11-20
• 00850068289073 - SFG Denuding pipettes: 2024-11-20