FDA UDI In Commercial Distribution 🇺🇸 United States

Elite

DI: 00810633021828 · Model: DK-300 · Biomedical Enterprises, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Elite
Primary DI
00810633021828
Version / Model
DK-300
Company Name
Biomedical Enterprises, Inc.
Labeler DUNS
792619009
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
3
Public Version Date
2020-05-07
Public Version Status
Update
Public Device Record Key
726af618-2080-4444-b3b2-cf65df52d65e

Device Description

Drill Kit For BME ELITE System

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
KDD Kit, Surgical Instrument, Disposable

GMDN Terms

Code Name
44052 Orthopaedic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 00810633021828

Customer Contacts

Phone
210-881-0064
Phone
210-881-0043

Device Sizes

Type Value Unit Text
Outer Diameter 3.0 Millimeter