Primary Device ID | 04035077219815 |
NIH Device Record Key | c5295bbd-6f22-4f18-b1e7-cc474bf0ab75 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 3M™ Adper™ Prompt™ L-Pop™ |
Version Model Number | 41928 |
Company DUNS | 315731711 |
Company Name | 3M Deutschland GmbH |
Device Count | 500 |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04035077219815 [Unit of Use] |
GS1 | 04064035145415 [Primary] |
GS1 | 04064035145422 [Primary] |
GS1 | 04064035145439 [Primary] |
KLE | AGENT, TOOTH BONDING, RESIN |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-24 |
Device Publish Date | 2024-04-16 |
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