| Primary Device ID | 10855683006736 |
| NIH Device Record Key | 261b2b62-4073-41e1-8541-7baa1e816de9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Timm Medical |
| Version Model Number | 57-05-144738 |
| Company DUNS | 002449593 |
| Company Name | PARKER LABORATORIES INC |
| Device Count | 1 |
| DM Exempt | false |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | 973-276-9500 |
| customerservice@parkerlabs.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00855683006739 [Primary] |
| GS1 | 10855683006736 [Package] Contains: 00855683006739 Package: Case [100 Units] In Commercial Distribution |
| KMJ | Lubricant, 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 | 2019-11-19 |
| Device Publish Date | 2019-11-11 |
| 20855683006542 - Ultradrape | 2023-09-26 Ultrasound Guided Peripheral Intravenous Barrier and Securement Device 3.25''x5.8'' |
| 20855683006917 - BrainScope | 2023-09-26 Skin Prep Gel 5g |
| 00855683006920 - 1% KCl GEL | 2022-06-13 Bulk packed 1% KCl gel |
| 00855683006883 - Alpha-Stim | 2022-03-09 Conducting solution |
| 00855683006890 - Alpha-Stim | 2022-03-09 Conducting Solution - 250 ml |
| 00855683006869 - Eclipse Probe Cover | 2022-01-10 A soft disposable ultrasound probe cover |
| 00855683006876 - Soterixmedical HD-Gel | 2021-11-30 High Definition Electrolyte Gel |
| 10855683006859 - BioWrap | 2021-10-19 BioWrap Conductive Cream |