FDA UDI In Commercial Distribution 🇺🇸 United States

GraftMag® Graft Delivery System

DI: 10840642171303 · Model: 10-7537 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GraftMag® Graft Delivery System
Primary DI
10840642171303
Version / Model
10-7537
Catalog Number
10-7537
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-23
Public Version
1
Public Version Date
2023-07-03
Public Version Status
New
Public Device Record Key
788561af-f1fa-4d44-b94d-f2ebbb6e2ed8

Device Description

Curved Cannula Obturator

Device Characteristics

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

Sterilization

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

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
33997 Surgical drill guide obturator

Identifiers

Type ID
Primary 10840642171303

Customer Contacts

Phone
203-944-9494