| Primary Device ID | 07613327063189 |
| NIH Device Record Key | 1d0131b4-2fb2-4719-9f19-a172e7b5de70 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 0620010101 |
| Catalog Number | 620-010-101 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327063189 [Primary] |
| HIG | INSUFFLATOR, HYSTEROSCOPIC |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327063189]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-23 |
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