| Primary Device ID | 07613327051537 |
| NIH Device Record Key | 3abb48b7-3e89-4838-8765-794b7d736e21 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 0233050065 |
| Catalog Number | 0233-050-065 |
| Company DUNS | 187502109 |
| Company Name | STRYKER CORPORATION |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(866)624-4422 |
| xx@xx.xx |
| Lumen/Inner Diameter | 5 Millimeter |
| Length | 10 Feet |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327051537 [Primary] |
| FCW | Light source, fiberoptic, routine |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327051537]
Moist Heat or Steam Sterilization;Ethylene Oxide;Hydrogen Peroxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |
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| 07613327271089 - DYNATRAN | 2024-10-29 COMPRESSOR |
| 07613327273885 - Aero-LL | 2024-10-29 INSERTER - DISTRACTOR |
| 37613327566162 - Neptune | 2024-10-23 V2 SPECIMEN COLLECTION MANIFOLD KIT |
| 07613327578577 - Target Tetra | 2024-10-08 Detachable Coil |
| 07613327578584 - Target Tetra | 2024-10-08 Detachable Coil |
| 07613327578591 - Target Tetra | 2024-10-08 Detachable Coil |
| 07613327578607 - Target Tetra | 2024-10-08 Detachable Coil |