Primary Device ID | 00810126041395 |
NIH Device Record Key | 314c4a16-552d-4a26-b46a-9d969bcf67eb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EK Pre-milled Abutment |
Version Model Number | EKPMA14MXNT |
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 | false |
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 | 00810126041395 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-25 |
Device Publish Date | 2025-02-17 |
00810126041418 | EKPMA14ZKNT |
00810126041401 | EKPMA14ZKHT |
00810126041395 | EKPMA14MXNT |
00810126041388 | EKPMA14MXHT |
00810126041371 | EKPMA14CANT |
00810126041364 | EKPMA14CAHT |
00810126041357 | EKPMA14ARNT |
00810126041340 | EKPMA14ARHT |
00810126041333 | EKPMA14ANNT |
00810126041326 | EKPMA14ANHT |
00810126041319 | EKPMA12CENT |
00810126041302 | EKPMA12CEHT |
00810126041296 | EKPMA10ZKNT |
00810126041289 | EKPMA10ZKHT |
00810126041272 | EKPMA10MXNT |
00810126041265 | EKPMA10MXHT |
00810126041258 | EKPMA10CANT |
00810126041241 | EKPMA10CAHT |
00810126041234 | EKPMA10ARNT |
00810126041227 | EKPMA10ARHT |
00810126041210 | EKPMA10ANNT |
00810126041203 | EKPMA10ANHT |
00810126041104 | ETPMA14CARHW |