Holding Pipette

GUDID 10805360017272

VITROLIFE INC.

User-induced micropipette

• Primary Device ID: 10805360017272
• NIH Device Record Key: cf84fa61-4521-4ab0-9d10-3c334209e919
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Holding Pipette
• Version Model Number: 15331
• Company DUNS: 051915038
• Company Name: VITROLIFE INC.
• Device Count: 10
• 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: false
• 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	00805360017275 [Unit of Use]
GS1	10805360017272 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K991104

FDA Product Code

• MQH: Microtools, Assisted Reproduction (Pipettes)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-04-21
• Device Publish Date: 2016-09-23

On-Brand Devices [Holding Pipette]

• 10805360018972: 15320
• 10805360018927: 15304
• 10805360017357: 15336
• 10805360017326: 15335
• 10805360017319: 15334
• 10805360017296: 15333
• 10805360017272: 15331
• 10805360017265: 15328
• 10805360017241: 15327
• 10805360017234: 15324
• 10805360017227: 15319
• 10805360017210: 15321
• 10805360017203: 15318
• 10805360017197: 15317
• 10805360017180: 15316
• 10805360017173: 15311
• 10805360017166: 15309
• 10805360017142: 15308
• 10805360017135: 15322
• 10805360017128: 15306
• 10805360017111: 15305
• 10805360017104: 15301
• 10805360017098: 15610
• 10805360017081: 15285
• 10805360017074: 15284