Primary Device ID | 00814913020297 |
NIH Device Record Key | 8b8a0cfe-049d-439d-8b9a-62d8c766d13c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET II Fixture SA Regular Pre-Mounted |
Version Model Number | AET2R4007S |
Company DUNS | 796083090 |
Company Name | HIOSSEN, INC. |
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 | 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 | 00814913020297 [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 | 2018-07-06 |
Device Publish Date | 2015-09-01 |
00814913020501 | AET2R5018S |
00814913020495 | AET2R5015S |
00814913020488 | AET2R5013S |
00814913020471 | AET2R5011S |
00814913020464 | AET2R5010S |
00814913020457 | AET2R5008S |
00814913020440 | AET2R5007S |
00814913020426 | AET2R4518S |
00814913020419 | AET2R4515S |
00814913020402 | AET2R4513S |
00814913020396 | AET2R4511S |
00814913020389 | AET2R4510S |
00814913020372 | AET2R4508S |
00814913020365 | AET2R4507S |
00814913020358 | AET2R4018S |
00814913020341 | AET2R4015S |
00814913020334 | AET2R4013S |
00814913020327 | AET2R4011S |
00814913020310 | AET2R4010S |
00814913020303 | AET2R4008S |
00814913020297 | AET2R4007S |