Welch Allyn, Inc. 33193-106-51

GUDID 00732094272178

Q-TEL MASTER 12 608MHz - AA Z230

WELCH ALLYN, INC.

Patient monitoring system central station monitor

• Primary Device ID: 00732094272178
• NIH Device Record Key: 1f19da28-b48a-4f54-aad3-057ce27fb61d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Welch Allyn, Inc.
• Version Model Number: 901145
• Catalog Number: 33193-106-51
• Company DUNS: 198227881
• Company Name: WELCH ALLYN, 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: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(315)685-2834
• Email: GDSN_SUPPORT@MYHILLROM.ONMICROSOFT.COM
• Phone: +1(315)685-2834
• Email: GDSN_SUPPORT@MYHILLROM.ONMICROSOFT.COM
• Phone: +1(315)685-2834
• Email: GDSN_SUPPORT@MYHILLROM.ONMICROSOFT.COM
• Phone: +1(315)685-2834
• Email: GDSN_SUPPORT@MYHILLROM.ONMICROSOFT.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00732094272178 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041607

FDA Product Code

• MHX: MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)

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: 2019-10-04
• Device Publish Date: 2019-09-26

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