BD Intermittent BUC10P

GUDID 16948796203919

Single-administration urethral drainage catheter

Primary Device ID	16948796203919
NIH Device Record Key	a0962560-5e89-4b1d-8297-a12c75bec5f0
Commercial Distribution Status	In Commercial Distribution
Brand Name	BD Intermittent
Version Model Number	BUC10P
Catalog Number	BUC10P
Company DUNS	528185295
Company Name	Hangzhou Bever Medical Devices Co., Ltd.
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	false
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

Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.
Special Storage Condition, Specify	Between 0 and 0 *Keep Away from Sunlight and Keep Dry.

Device Issuing Agency	Device ID
GS1	06948796203912 [Primary]
GS1	16948796203919 [Package] Contains: 06948796203912 Package: CA [30 Units] In Commercial Distribution
GS1	26948796203916 [Package] Package: BX [300 Units] In Commercial Distribution

GBM	Catheter, Urethral

Steralize Prior To Use	false
Device Is Sterile	true

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16948796204022	BD Ready-To-Use Hydrophilic Catheter
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16948796204008	BD Ready-To-Use Hydrophilic Catheter
16948796203995	BD Ready-To-Use Hydrophilic Catheter
16948796203988	BD Ready-To-Use Hydrophilic Catheter
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16948796203964	BD Ready-To-Use Hydrophilic Catheter
16948796203957	BD Ready-To-Use Hydrophilic Catheter