FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00840085224799 · Model: GB224518C · HYHTE HOLDINGS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00840085224799
Version / Model
GB224518C
Catalog Number
GB224518C
Company Name
HYHTE HOLDINGS, INC.
Labeler DUNS
073029645
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-08
Public Version
1
Public Version Date
2021-07-16
Public Version Status
New
Public Device Record Key
9f1a9b3e-a253-4738-bf6a-41f09ab70b78

Device Description

LLIF SPACER

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
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar
KWQ Appliance, Fixation, Spinal Intervertebral Body
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00840085224799

Customer Contacts

Phone
7608148047

Device Sizes

Type Value Unit Text
Width 22 Millimeter
Height 18 Millimeter
Angle 12 degree
Length 45 Millimeter