FDA UDI In Commercial Distribution 🇺🇸 United States

Implant Remover

DI: 08809476189941 · Model: IRFS · EBI Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Implant Remover
Primary DI
08809476189941
Version / Model
IRFS
Company Name
EBI Inc.
Labeler DUNS
689515003
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-02
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
afaa6c07-5adb-4dd6-a77f-fe4bc6e7a2c1

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EJB Handle, Instrument, Dental

GMDN Terms

Code Name
55847 Dental implant system

Identifiers

Type ID
Primary 08809476189941