HEINE BETA® 200 C-002.30.100

GUDID 04053755120208

Heine Optotechnik GmbH & Co. KG

Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Aneroid manual sphygmomanometer Direct ophthalmoscope Direct ophthalmoscope Direct ophthalmoscope Direct ophthalmoscope Direct ophthalmoscope Direct ophthalmoscope Direct ophthalmoscope Direct ophthalmoscope

• Primary Device ID: 04053755120208
• NIH Device Record Key: f008e6cc-dcf2-4688-8e2f-6df6cbdb618d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HEINE BETA® 200
• Version Model Number: 000
• Catalog Number: C-002.30.100
• Company DUNS: 315274563
• Company Name: Heine Optotechnik GmbH & Co. KG
• 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: false
• 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

Customer Support Contacts

• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com
• Phone: +1 (603) 742-7103
• Email: service@heine-na.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04053755120208 [Primary]

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive
• HLJ: Ophthalmoscope, Battery-Powered

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

On-Brand Devices [HEINE BETA® 200 ]

• 04053755120222: 310
• 04053755120208: 000