FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00840085220753 · Model: KZB060013 · HYHTE HOLDINGS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00840085220753
Version / Model
KZB060013
Catalog Number
KZB060013
Company Name
HYHTE HOLDINGS, INC.
Labeler DUNS
073029645
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-30
Public Version
1
Public Version Date
2021-08-09
Public Version Status
New
Public Device Record Key
ec955a99-262b-412e-b479-7a8d2ca15877

Device Description

SCREW GUIDE, HALF AND FULL PLATE, 13MM

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

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 00840085220753

Customer Contacts

Phone
7608148047

Device Sizes

Type Value Unit Text
Height 13 Millimeter