Primary Device ID | 10724995161559 |
NIH Device Record Key | 7534dd74-e9cd-41f9-a6ed-ff861fe10251 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Celerity |
Version Model Number | LCB049 |
Catalog Number | LCB049 |
Company DUNS | 961394798 |
Company Name | STERIS CORPORATION |
Device Count | 25 |
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 | false |
Serial Number | true |
Manufacturing Date | false |
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 | true |
Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
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Phone | +1(800)548-4873 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00724995161552 [Unit of Use] |
GS1 | 10724995161559 [Primary] |
FRC | Indicator, biological sterilization process |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-04-01 |
Device Publish Date | 2019-06-14 |
00724995154257 | The Celerity HP Incubator was designed exclusively to incubate and read activated Celerity 20 HP |
10724995161573 | The Celerity 20 STEAM Process Challenge Device for Gravity Cycles is for routine monitoring, qua |
10724995161566 | The Celerity 20 STEAM Process Challenge Device for Dynamic Air Removal Cycles has 25 packs with |
10724995161559 | The Celerity 20 STEAM Process Challenge Device for Dynamic Air Removal Cycles has 25 packs with |
10724995161542 | The Celerity 20 STEAM Biological Indicator is a fast read 20-minute BI used for routine monitor |
00724995161583 | The Celerity STEAM Incubator is designed to incubate and automatically read the Celerity 20 STEA |
10724995161597 | The Celerity 20 HP Challenge Pack is intended for qualification testing of the V-PRO Low Tempera |
10724995167759 | The Celerity Xtend 10 Assembly with a Celerity 20 STEAM Biological Indicator and a Celerity 10 S |
10724995154230 | The Celerity 20 HP Biological Indicator is used with the V-PRO Low Temperature Sterilization Sys |
00724995203405 | The Celerity 20 STEAM Biological Indicator for IUSS is used to monitor the critical parameters o |
00724995201852 | The Celerity STEAM Incubator is designed to incubate and automatically read the Celerity 20 STEA |
00724995215941 | The Celerity Incubator is used to incubate and automatically read STERIS Celerity Biological Ind |
00724995215934 | The Celerity 5 HP Challenge Pack is intended for qualification testing of the V-PRO Low Temperat |
00724995215927 | The Celerity 5 HP Biological Indicator is used for routine monitoring of certain cycles of the V |