Primary Device ID | 07332747113518 |
NIH Device Record Key | 56b28abf-9b38-4b12-9d6c-e1435668c790 |
Commercial Distribution Discontinuation | 2018-06-12 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 38716 |
Catalog Number | 38716 |
Company DUNS | 353939929 |
Company Name | Nobel Biocare AB |
Device Count | 1 |
DM Exempt | true |
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 | false |
Manufacturing Date | false |
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 |
Phone | +1(800)322-5001 |
us.customerservice@nobelbiocare.com |
Height | 0.3 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07332747113518 [Primary] |
NHA | ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07332747113518]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 7 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2017-10-25 |
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