| Primary Device ID | 00612649170282 |
| NIH Device Record Key | ac000ef0-54a3-4ce7-a4b6-124aea9a39c7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ADULT ULTRA FLEX® |
| Version Model Number | 81213B-61Z |
| Catalog Number | 81213B-61Z |
| Company DUNS | 009299017 |
| Company Name | King Systems Corporation |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00612649170282 [Package] Contains: 00612649191256 Package: [20 Units] In Commercial Distribution |
| GS1 | 00612649191256 [Primary] |
| CAI | Circuit, breathing (w connector, adaptor, y piece) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-29 |
| Device Publish Date | 2020-10-21 |
| 00612649214696 | ADULT ULTRAFLEX CIRCUIT |
| 00612649215129 | ADULT ULTRAFLEX CIRCUIT |
| 00612649141596 | ADULT ULTRAFLEX CIRCUIT |
| 00612649158754 | ADULT ULTRAFLEX CIRCUIT |
| 00612649148861 | ADULT ULTRAFLEX CIRCUIT |
| 00612649172583 | ADULT ULTRAFLEX CIRCUIT |
| 00612649158723 | ADULT ULTRAFLEX CIRCUIT |
| 00612649170282 | ADULT ULTRAFLEX CIRCUIT |
| 00612649135717 | ADULT ULTRAFLEX CIRCUIT |
| 00612649215631 | ADULT ULTRAFLEX CIRCUIT |
| 00612649215617 | ADULT ULTRAFLEX CIRCUIT |
| 00612649215679 | ADULT ULTRA FLEX CIRCUIT PACK KIT |
| 00612649215587 | ADULT ULTRAFLEX PACK KIT |
| 00612649215501 | ADULT ULTRAFLEX CIRCUIT |
| 00612649215938 | ADULT ULTRAFLEX CIRCUIT |
| 00612649215761 | ADULT ULTRAFLEX CIRCUIT |
| 00612649215976 | ADULT ULTRAFLEX CIRCUIT |
| 00612649215952 | ADULT ULTRAFLEX CIRCUIT |
| 00612649216249 | ADULT ULTRAFLEX CIRCUIT |