| Primary Device ID | 00889024015050 |
| NIH Device Record Key | 0ce166fa-f63c-4d07-93dd-58fa84fd382f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tapered Screw-Vent Implant System |
| Version Model Number | HC445 |
| Company DUNS | 103167086 |
| Company Name | ZIMMER DENTAL INC. |
| 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 | false |
| Labeled No Natural Rubber Latex | false |
| 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 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 | 00889024015050 [Primary] |
| NHA | ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2015-10-23 |
| 00889024019126 | TSF |
| 00889024019072 | TSB |
| 00889024019065 | TS |
| 00889024016569 | PSAZH4RML |
| 00889024016552 | PSAZH4RM |
| 00889024016545 | PSAZH4RFL |
| 00889024016538 | PSAZH4RF |
| 00889024016521 | PSAZH4MRM |
| 00889024016514 | PSAZH4M |
| 00889024016507 | PSAZH4L |
| 00889024016491 | PSAZH4 |
| 00889024016484 | PSAZH3RML |
| 00889024016477 | PSAZH3RM |
| 00889024016460 | PSAZH3RFL |
| 00889024016453 | PSAZH3RF |
| 00889024016446 | PSAZH3MRM |
| 00889024016439 | PSAZH3M |
| 00889024016422 | PSAZH3L |
| 00889024016415 | PSAZH3 |
| 00889024016408 | PSATH5RML |
| 00889024016392 | PSATH5RM |
| 00889024016385 | PSATH5RFL |
| 00889024016378 | PSATH5RF |
| 00889024016361 | PSATH5MRM |
| 00889024016347 | PSATH5L |
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| 00889024016309 | PSATH4RFL |
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| 00889024016224 | PSATH3RFL |
| 00889024016200 | PSATH3MRM |
| 00889024016187 | PSATH3L |
| 00889024015050 | HC445 |
| 00889024013766 | AHS |
| 00889024021020 | ZOCHEAL6S |
| 00889024021013 | ZOCHEAL6A |
| 00889024021006 | ZOCHEAL5S |
| 00889024020993 | ZOCHEAL5A |
| 00889024016590 | PT341A |