Primary Device ID | 00810125995644 |
NIH Device Record Key | 12f257eb-490f-4c58-943e-1ded6957128d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET Multi Angled Abutment |
Version Model Number | ET17MAM4840CWH |
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 | 00810125995644 [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 | 2024-07-01 |
Device Publish Date | 2024-06-21 |
00814913028750 | ETMA530SHW |
00814913028743 | ETMA430SHW |
00814913028736 | ETMA330SHW |
00814913028729 | ETMA417SHW |
00814913028712 | ETMA317SHW |
00814913028705 | ETMA217SHW |
00814913028699 | ETMA530MHW |
00814913028682 | ETMA430MHW |
00814913028675 | ETMA330MHW |
00814913028668 | ETMA417MHW |
00814913028651 | ETMA317MHW |
00814913028644 | ETMA217MHW |
00810125999116 | ETMA517SHW |
00810125995736 | ET30MAS4850CWH |
00810125995729 | ET30MAS4840CWH |
00810125995712 | ET30MAS4830CWH |
00810125995705 | ET17MAS4840CWH |
00810125995699 | ET17MAS4830CWH |
00810125995682 | ET17MAS4820CWH |
00810125995675 | ET30MAM4850CWH |
00810125995668 | ET30MAM4840CWH |
00810125995651 | ET30MAM4830CWH |
00810125995644 | ET17MAM4840CWH |
00810125995637 | ET17MAM4830CWH |
00810125995620 | ET17MAM4820CWH |