FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00840085239359 · Model: LZFMBA12C · HYHTE HOLDINGS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00840085239359
Version / Model
LZFMBA12C
Catalog Number
LZFMBA12C
Company Name
HYHTE HOLDINGS, INC.
Labeler DUNS
073029645
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-27
Public Version
2
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
82431599-21d0-4be6-93da-20d9bba6d004

Device Description

ZERO PLATE TRIAL RASP

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

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00840085239359

Customer Contacts

Phone
7608148047

Device Sizes

Type Value Unit Text
Width 16 Millimeter
Length 14 Millimeter
Height 12 Millimeter
Angle 13 degree