FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00840085238604 · Model: LZFLAB09D · HYHTE HOLDINGS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00840085238604
Version / Model
LZFLAB09D
Catalog Number
LZFLAB09D
Company Name
HYHTE HOLDINGS, INC.
Labeler DUNS
073029645
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-26
Public Version
2
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
b1bb3d9e-3fb7-4932-bf2e-269b76d0114c

Device Description

HALF PLATE TRIAL

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
ODP Intervertebral Fusion Device With Bone Graft, Cervical
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00840085238604

Customer Contacts

Phone
7608148047

Device Sizes

Type Value Unit Text
Width 18 Millimeter
Length 15 Millimeter
Height 9 Millimeter
Angle 15 degree