Primary Device ID | 00810988030889 |
NIH Device Record Key | 2bf4cb7f-8a90-4de3-b1c7-91b19b89c35b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | QUALITY PLUS |
Version Model Number | PBM02 |
Catalog Number | PBM02 |
Company DUNS | 079723355 |
Company Name | HANDPIECE PARTS & REPAIRS, 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810988030889 [Primary] |
EFB | Handpiece, Air-Powered, Dental |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00810988030889]
Moist Heat or Steam Sterilization
[00810988030889]
Moist Heat or Steam Sterilization
[00810988030889]
Moist Heat or Steam Sterilization
[00810988030889]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-30 |
Device Publish Date | 2022-05-20 |
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