MOBILE INSTRUMENT

GUDID B150QW2201M0

NURSE ASSIST, INC.

Electrical-only medical device connection cable, reusable Electrical-only medical device connection cable, reusable

• Primary Device ID: B150QW2201M0
• NIH Device Record Key: 9fb8ea74-6244-4bad-8818-1ff10da67eb6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MOBILE INSTRUMENT
• Version Model Number: QW2201M
• Company DUNS: 869434464
• Company Name: NURSE ASSIST, INC.
• Device Count: 1
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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
HIBCC	B150QW2201M0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K942194

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2016-11-07

On-Brand Devices [MOBILE INSTRUMENT]

• B150QW2201M0: QW2201M
• B150QS2103M0: QS2103M
• B150QS2102M0: QS2102M
• B150QS2101M0: QS2101M
• B150QI2900M0: QI2900
• B150QI2407M0: QI2407M
• B150QI2401M0: QI2401M
• B150QI2301M0: QI2301M
• B150QI1004M0: QI1004M
• B150QI1003M0: QI1003M
• B150QI1002M0: QI1002M