Primary Device ID | 00858653006630 |
NIH Device Record Key | 95e5581e-081f-4025-9746-3c53901bbc85 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BANZAI DPA Firm White 4-Web Cup |
Version Model Number | Firm White |
Catalog Number | AM-3002 |
Company DUNS | 180611519 |
Company Name | AMERICAN MEDICAL & HOSPITAL SUPPLY CO., 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 | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 00858653006630 [Primary] |
EGS | Handpiece, Contra- And Right-Angle Attachment, Dental |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-24 |
Device Publish Date | 2020-01-16 |
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