Primary Device ID | 04012030021081 |
NIH Device Record Key | 479bcca8-1d66-4612-9577-b78c7a403f44 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | seca 442 |
Version Model Number | 442 |
Catalog Number | 4420000009 |
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 | |
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 | 04012030021081 [Primary] |
FRW | SCALE, 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 | 2024-05-15 |
Device Publish Date | 2024-05-07 |
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