Primary Device ID | 04012030018821 |
NIH Device Record Key | beebf4c1-3767-48ee-b235-1fd3cd5aa9e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | seca 700 |
Version Model Number | 700 |
Catalog Number | 7001121993 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04012030018821 [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 | 2020-01-08 |
Device Publish Date | 2019-12-31 |
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