| Primary Device ID | 04012030014519 |
| NIH Device Record Key | 1e94d617-d6d3-4c74-8224-3aa00193e092 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | seca 418 |
| Version Model Number | 418 |
| Catalog Number | 4180000004 |
| Company DUNS | 316584937 |
| Company Name | seca 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 | true |
| 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(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com | |
| Phone | +1(800)5427322 |
| info.us@seca.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04012030014519 [Primary] |
| FRI | SCALE, STAND-ON, PATIENT |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-08 |
| Device Publish Date | 2020-08-31 |
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