| Primary Device ID | 04053755136759 |
| NIH Device Record Key | 37c487bb-dd7a-49f5-8da7-71ab5e29c32e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HEINE GAMMA® Single-tube cuff |
| Version Model Number | 000 |
| Catalog Number | M-000.09.619 |
| 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 |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com | |
| Phone | +1 (603) 742-7103 |
| service@heine-na.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04053755136759 [Primary] |
| DXQ | Blood Pressure Cuff |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-07-22 |
| Device Publish Date | 2016-09-24 |
| 04053755136964 | 000 |
| 04053755136940 | 000 |
| 04053755136926 | 000 |
| 04053755136759 | 000 |
| 04053755136742 | 000 |