FDA UDI In Commercial Distribution 🇺🇸 United States

Embosphere®

DI: 00884450403174 · Model: 00884450403174 · BIOSPHERE MEDICAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Embosphere®
Primary DI
00884450403174
Version / Model
00884450403174
Catalog Number
S210GH/C
Company Name
BIOSPHERE MEDICAL
Labeler DUNS
635091932
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-13
Public Version
2
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
e3b18487-9caf-48aa-875c-435c97eb8abc

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KRD Device, Vascular, for Promoting Embolization

GMDN Terms

Code Name
60938 Embolization particle, non-bioabsorbable

Identifiers

Type ID
Package 10884450403171
Primary 00884450403174

Device Sizes

Type Value Unit Text
Device Size Text, specify Size Range-100-300 µm