| Primary Device ID | 20840935107566 |
| NIH Device Record Key | d49267e7-370a-4ecd-be58-576924d24be0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Disposable cuff |
| Version Model Number | 98-0700-05 |
| Company DUNS | 148191133 |
| Company Name | SUNTECH MEDICAL, 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 | true |
| 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 |
| Phone | 1-919-654-2300 |
| UDI_MAIL@suntechmed.com | |
| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
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| Phone | 1-919-654-2300 |
| UDI_MAIL@suntechmed.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10840935107569 [Primary] |
| GS1 | 20840935107566 [Package] Contains: 10840935107569 Package: Box [20 Units] In Commercial Distribution |
| DXQ | Blood Pressure Cuff |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-07-22 |
| Device Publish Date | 2017-05-25 |