Primary Device ID | J014600410621 |
NIH Device Record Key | 975236bc-503f-4e6a-8c16-9f9072bbfd8e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FLEXITIME MEDIUM FLOW 1 X (2 X 50 ML) |
Version Model Number | 60041062 |
Catalog Number | 60041062 |
Company DUNS | 315666321 |
Company Name | Heraeus Kulzer GmbH |
Device Count | 1 |
DM Exempt | true |
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 | 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 |
Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Phone | +1(800)431-1785 |
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Device Issuing Agency | Device ID |
---|---|
HIBCC | J014600410621 [Primary] |
ELW | MATERIAL, IMPRESSION |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-10-30 |
Device Publish Date | 2016-09-23 |
J014600410621 | Dental Composite resin |
J014600410620 | Material Impression |
J014400050410 | Material, Impression |