Primary Device ID | 06947600300335 |
NIH Device Record Key | f4986373-be16-4789-b5b1-25c716b30238 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Standard Implant |
Version Model Number | 013110 |
Company DUNS | 527603266 |
Company Name | BIO CONCEPT 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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06947600300335 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-11-19 |
Device Publish Date | 2016-09-01 |
06947600300427 | 013200 |
06947600300410 | 013190 |
06947600300403 | 013180 |
06947600300380 | 013160 |
06947600300373 | 013150 |
06947600300366 | 013140 |
06947600300359 | 013130 |
06947600300335 | 013110 |
06947600300328 | 013100 |
06947600300311 | 013090 |
06947600300304 | 013080 |
06947600300298 | 013070 |
06947600300274 | 013050 |
06947600300267 | 013040 |
06947600300250 | 013030 |
06947600300243 | 013020 |
06947600300236 | 013010 |