FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00841379173151 · Model: AJHA95040 · HYHTE HOLDINGS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00841379173151
Version / Model
AJHA95040
Catalog Number
AJHA95040
Company Name
HYHTE HOLDINGS, INC.
Labeler DUNS
073029645
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-27
Public Version
1
Public Version Date
2021-06-04
Public Version Status
New
Public Device Record Key
b727e6db-79da-4d10-b0c0-175805aa898a

Device Description

LRG DIA CORTICAL POLYAXIAL SCREW, CANN, SELF CUTTING

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
NKB Thoracolumbosacral Pedicle Screw System
KWP Appliance, Fixation, Spinal Interlaminal
OLO Orthopedic Stereotaxic Instrument

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00841379173151

Customer Contacts

Phone
7608148047

Device Sizes

Type Value Unit Text
Length 40 Millimeter
Outer Diameter 9.5 Millimeter