Primary Device ID | 00628504370209 |
NIH Device Record Key | db71370a-1342-4e86-a1cc-3d8ef92dea57 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AirLight M800P |
Version Model Number | HP3036P |
Company DUNS | 244261462 |
Company Name | Beyes Dental Canada 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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
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 | 00628504370209 [Primary] |
EFB | Handpiece, Air-Powered, Dental |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00628504370209]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-22 |
Device Publish Date | 2019-04-12 |
00628504370803 | M800P-S/K, KaVo Backend, Standard Head, Triple Spray, Direct-LED |
00628504370797 | M800P-S/W, W&H Backend, Standard Head, Triple Spray, Direct-LED |
00628504370780 | M800P-S/N, NSK Backend, Standard Head, Triple Spray, Direct-LED |
00628504370773 | M800P-S/PD, Beyes PD Backend, Standard Head, Triple Spray, Direct-LED |
00628504370766 | M800P-S/QD, Beyes QD Backend, Standard Head, Triple Spray, Direct-LED |
00628504370322 | M800P-M/PD, Beyes PD Backend, Triple Spray, Direct-LED |
00628504370278 | M800P-M/ST, STAR Backend, Triple Spray, Direct-LED |
00628504370230 | M800P-M/N, NSK Backend, Triple Spray, Direct-LED |
00628504370209 | M800P-M/K, KaVo Backend, Triple Spray, Direct-LED |
00628504370193 | M800P-M/W, W&H Backend, Triple Spray, Direct-LED |
00628504370162 | M800P-M/M4, M4 Backend, Triple Spray, Direct-LED |