Embosphere® V220GH/B

GUDID 10884450403713

BIOSPHERE MEDICAL

Embolization particle, non-bioabsorbable
Primary Device ID10884450403713
NIH Device Record Key3a46c6df-3311-428e-b96f-647018825754
Commercial Distribution StatusIn Commercial Distribution
Brand NameEmbosphere®
Version Model Number00884450403716
Catalog NumberV220GH/B
Company DUNS635091932
Company NameBIOSPHERE MEDICAL
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100884450403716 [Primary]
GS110884450403713 [Package]
Contains: 00884450403716
Package: [5 Units]
In Commercial Distribution

FDA Product Code

KRDDevice, Vascular, for Promoting Embolization

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-10
Device Publish Date2022-10-01

On-Brand Devices [Embosphere®]

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1088445040344700884450403440
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1088445040342300884450403426
1088445040313300884450403136
1088445040294500884450402948
1088445040305800884450403051
1088445029943900884450299432
1088445040382900884450403822
1088445040371300884450403716

Trademark Results [Embosphere]

Mark Image

Registration | Serial
Company
Trademark
Application Date
EMBOSPHERE
EMBOSPHERE
74392090 1883442 Live/Registered
BIOSPHERE MEDICAL INC.
1993-05-19

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