FDA UDI In Commercial Distribution 🇺🇸 United States

Occlusin 500

DI: 07540270000056 · Model: Ekobi 503L · IMBiotechnologies Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Occlusin 500
Primary DI
07540270000056
Version / Model
Ekobi 503L
Company Name
IMBiotechnologies Ltd
Labeler DUNS
244234295
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-24
Public Version
3
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
8f3e2743-d861-4ca9-9a1b-e5fe1c45d557

Device Description

Occlusin 500 is a family of biodegradable dense microspheres which are available in a range of calibrated sizes. The poly-DL-lactic-co-glycolic acid (PLGA) microspheres are surface-coated with bovine collagen. Following injection, the collagen binds patient platelets resulting in a platelet-rich clot which occludes the vasculature. The microspheres slowly degrade and are removed from the body over 4-6 months.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
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
59048 Embolization particle, bioabsorbable

Identifiers

Type ID
Primary 07540270000056

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K093813 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 180-212 µm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry location