Primary Device ID | 08806388267217 |
NIH Device Record Key | 8d8dafe7-8a16-4434-9ce3-db2ab3d10c6d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Implant Carrier |
Version Model Number | ICRO2127 |
Catalog Number | ICRO2127 |
Company DUNS | 687388178 |
Company Name | Megagen Implant Co. Ltd |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08806388267217 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08806388267217]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-01-09 |
Device Publish Date | 2019-11-22 |
08806388267217 | Octa 2.1/ Regular |
08806388267200 | Octa 2.5/ Regular |
08806388220380 | ST Regular/ Hex2.1 |
08806388220373 | Common Narrow/ Hex1.7 |
08809728993845 | R2 Octa 2.5/ Regular |
08809728993838 | R2 Octa 2.1/ Regular |
08809854020002 | Common Narrow/ Hex2.3 |
08809931181534 | ICWO2530 |
08809931181527 | ICWO2530H |
08806388262526 | ICWH2711CT |
08806388262519 | ICRH2221CT |
08806388262502 | ICWH2538OS |
08806388262496 | ICRH2127OS |
08806388270422 | ICWT43RT |
08806388270378 | ICWT50RT |
08806388270361 | ICRT35RT |
08806388262489 | ICWH2624 |
08806388246489 | ICRSBLH |
08806388246472 | ICRSBNH |
08806388246465 | ICRSBL2 |
08806388246458 | ICRSBN |
08806388244522 | ICRH2523O |
08806388244515 | ICRH2523HO |