FDA UDI In Commercial Distribution 🇺🇸 United States

Reform Pedicle Screw System

DI: 00840019928595 · Model: 39-SP-0001 · PRECISION SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Reform Pedicle Screw System
Primary DI
00840019928595
Version / Model
39-SP-0001
Catalog Number
39-SP-0001
Company Name
PRECISION SPINE, INC.
Labeler DUNS
079398589
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-29
Public Version
1
Public Version Date
2019-06-06
Public Version Status
New
Public Device Record Key
1807df4b-8b66-4dc1-be85-9f7ad9dc88e5

Device Description

Bone Awl

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWJ Awl

GMDN Terms

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

Identifiers

Type ID
Primary 00840019928595