Primary Device ID | 08800026102281 |
NIH Device Record Key | c45f7f2e-9364-4e82-bd19-174f376f9b33 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IU Healing Abutment |
Version Model Number | IUHA4040A |
Company DUNS | 688857820 |
Company Name | WARANTEC.Co.,Ltd |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800026102281 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-20 |
Device Publish Date | 2023-04-12 |
08800026106036 | IUHA6060 |
08800026102533 | IUHA6050 |
08800026102526 | IUHA6040 |
08800026102519 | IUHA6030 |
08800026102502 | IUHA6020 |
08800026102496 | IUHA6010 |
08800026102489 | IUHA5060 |
08800026102472 | IUHA5050 |
08800026102465 | IUHA5040 |
08800026102458 | IUHA5030 |
08800026102441 | IUHA5020 |
08800026102434 | IUHA5010 |
08800026102427 | IUHA4060 |
08800026102410 | IUHA4050 |
08800026102403 | IUHA4040 |
08800026102397 | IUHA4030 |
08800026102380 | IUHA4020 |
08800026102373 | IUHA4010 |
08800026102366 | IUHA5060A |
08800026102359 | IUHA5050A |
08800026102342 | IUHA5040A |
08800026102335 | IUHA5030A |
08800026102328 | IUHA5020A |
08800026102311 | IUHA5010A |
08800026102304 | IUHA4060A |
08800026102298 | IUHA4050A |
08800026102281 | IUHA4040A |
08800026102274 | IUHA4030A |
08800026102267 | IUHA4010A |
08800026102243 | IUHA4020A |