Primary Device ID | 07323190093021 |
NIH Device Record Key | aafef010-8797-454a-af3b-0f5a3f1556c7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biogel® Indicator® System |
Version Model Number | 31285 |
Company DUNS | 631770658 |
Company Name | Mölnlycke Health Care AB |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07323190092857 [Primary] |
GS1 | 07323190093014 [Package] Contains: 07323190092857 Package: PACK_OR_INNER_PACK [50 Units] In Commercial Distribution |
GS1 | 07323190093021 [Package] Contains: 07323190093014 Package: CASE [4 Units] In Commercial Distribution |
KGO | Surgeon's gloves |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-31 |
Device Publish Date | 2022-10-21 |
07323190093045 | Biogel Indicator Underglove 9.0 x 40 |
07323190093021 | Biogel Indicator Underglove 8.5 x 50 |
07323190092994 | Biogel Indicator Underglove 8.0 x 50 |
07323190092956 | Biogel Indicator Underglove 7.5 x 50 |
07323190092918 | Biogel Indicator Underglove 7.0 x 50 |
07323190092697 | Biogel Indicator Underglove 6.5 x 50 |
07323190085484 | Biogel Indicator Underglove 6.0 x 50 |
07323190085453 | Biogel Indicator Underglove 5.5 x 50 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BIOGEL 87684161 not registered Dead/Abandoned |
PHOENIX Chemical, Inc. 2017-11-14 |
BIOGEL 86217294 4730182 Live/Registered |
Phoenix Chemical Inc. 2014-03-11 |
BIOGEL 85595270 4389014 Live/Registered |
Louis Garneau Sports Inc. 2012-04-11 |
BIOGEL 85481846 4315606 Dead/Cancelled |
Rothbard, Michael 2011-11-28 |
BIOGEL 78473714 not registered Dead/Abandoned |
IVREA Inc. 2004-08-25 |
BIOGEL 78135510 3013748 Dead/Cancelled |
REGENT MEDICAL LIMITED 2002-06-13 |
BIOGEL 77858173 not registered Dead/Abandoned |
Meynard Designs, Inc. 2009-10-27 |
BIOGEL 77565224 4523726 Live/Registered |
Summers, Adam N 2008-09-09 |
BIOGEL 77157241 not registered Dead/Abandoned |
Lincoln L. Neal 2007-04-16 |
BIOGEL 76639768 not registered Dead/Abandoned |
Electromed, Inc. 2005-05-31 |
BIOGEL 76626918 3254405 Dead/Cancelled |
Phoenix Chemical Inc. 2005-01-04 |
BIOGEL 75133602 2128295 Live/Registered |
REGENT MEDICAL LIMITED 1996-07-12 |