| Primary Device ID | 05060097933815 | 
| NIH Device Record Key | 014bd0fb-4b76-4ad8-8f3e-89552e071d78 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Biogel Sensor® | 
| Version Model Number | 30655 | 
| 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 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 | 05060097933730 [Primary] | 
| GS1 | 05060097933815 [Package] Contains: 05060097933730 Package: PACK_OR_INNER_PACK [50 Units] In Commercial Distribution | 
| GS1 | 05060097933891 [Package] 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 | 
| 05060097933969 | Biogel Sensor 9.0 x 40 US | 
| 05060097933877 | Biogel Sensor 8.5 x 50 US | 
| 05060097933945 | Biogel Sensor 8.0 x 50 US | 
| 05060097933853 | Biogel Sensor 7.5 x 50 US | 
| 05060097933846 | Biogel Sensor 7.0 x 50 US | 
| 05060097933914 | Biogel Sensor 6.5 x 50 US | 
| 05060097933907 | Biogel Sensor 6.0 x 50 US | 
| 05060097933815 | Biogel Sensor 5.5 x 50 US | 
| 05060097932511 | Biogel Super Sensitive 9.0x40 US EUR | 
| 05060097932504 | Biogel Super Sensitive 8.5x50 US EUR | 
| 05060097932498 | Biogel Super Sensitive 8.0x50 US EUR | 
| 05060097932481 | Biogel Super Sensitive 7.5x50 US EUR | 
| 05060097932474 | Biogel Super Sensitive 7.0x50 US EUR | 
| 05060097932542 | Biogel Super Sensitive 6.5x50 US EUR | 
| 05060097932535 | Biogel Super Sensitive 6.0x50 US EUR | 
| 05060097932528 | Biogel Super Sensitive 5.5x50 US EUR | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  BIOGEL SENSOR  74408371  1922868 Live/Registered | REGENT MEDICAL LIMITED 1993-07-02 |