Primary Device ID | 50724995164053 |
NIH Device Record Key | 8b51deaf-5146-4357-9c9f-69c3dc04bb29 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 886127 |
Catalog Number | 886127 |
Company DUNS | 961394798 |
Company Name | STERIS CORPORATION |
Device Count | 50 |
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 | 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 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Width | 8 Inch |
Length | 21 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00724995164058 [Unit of Use] |
GS1 | 10724995164055 [Primary] |
GS1 | 50724995164053 [Package] Contains: 10724995164055 Package: Case [2 Units] In Commercial Distribution |
FRG | Wrap, sterilization |
JOJ | Indicator, physical/chemical sterilization process |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2019-06-21 |
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