Primary Device ID | 15901549097198 |
NIH Device Record Key | 15a93f1f-081a-492c-b6fa-5d6f98449e19 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MediSafe Solo, safety lancet |
Version Model Number | 23G |
Catalog Number | 7140 |
Company DUNS | 422528088 |
Company Name | HTL STREFA S A |
Device Count | 200 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +48422700010 |
info@htl-strefa.com | |
Phone | +48422700010 |
info@htl-strefa.com | |
Phone | +48422700010 |
info@htl-strefa.com | |
Phone | +48422700010 |
info@htl-strefa.com | |
Phone | +48422700010 |
info@htl-strefa.com | |
Phone | +48422700010 |
info@htl-strefa.com | |
Phone | +48422700010 |
info@htl-strefa.com | |
Phone | +48422700010 |
info@htl-strefa.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05901549097191 [Primary] |
GS1 | 15901549097198 [Package] Contains: 05901549097191 Package: shipper [10 Units] In Commercial Distribution |
GS1 | 85901549097197 [Unit of Use] |
FMK | Lancet, Blood |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-11-09 |
Device Publish Date | 2020-10-30 |
85901549097203 | Sterile,single-use safety lancets for capillary blood sampling. |
15901549097198 | Sterile,single-use safety lancets for capillary blood sampling |