FDA UDI In Commercial Distribution 🇺🇸 United States

GOEZ 2.0 6.5 COMPLETE KIT

DI: 00810012485241 · Model: 20045 · BIOPRO, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GOEZ 2.0 6.5 COMPLETE KIT
Primary DI
00810012485241
Version / Model
20045
Company Name
BIOPRO, INC.
Labeler DUNS
618749857
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-06
Public Version
1
Public Version Date
2019-06-14
Public Version Status
New
Public Device Record Key
42729ba5-4b21-4de9-8c74-fa0be9a84762

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 00810012485241

Premarket Submissions

Submission Number Supplement Number
K083490 000