Primary Device ID | J021063649001 |
NIH Device Record Key | 2146bcc3-a0dc-4f62-88bc-f8f279159476 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Scaler Tip 3Pr |
Version Model Number | 06364900 |
Company DUNS | 300238441 |
Company Name | W & H Dentalwerk Bürmoos GmbH |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | J021063649001 [Primary] |
ELC | Scaler, Ultrasonic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
[J021063649001]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-27 |
Device Publish Date | 2023-07-19 |
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