FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00840085235115 · Model: LZA980000-12 · HYHTE HOLDINGS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00840085235115
Version / Model
LZA980000-12
Catalog Number
LZA980000-12
Company Name
HYHTE HOLDINGS, INC.
Labeler DUNS
073029645
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-28
Public Version
2
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
519ba8c8-bee8-41b9-aa84-d34fcee37a80

Device Description

ZERO PLATE TRIAL CADDY, LARGE

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
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 00840085235115

Customer Contacts

Phone
760-814-8047

Device Sizes

Type Value Unit Text
Angle 7 degree