FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00841379130802 · Model: AA3A75035 · HYHTE HOLDINGS, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00841379130802
Version / Model
AA3A75035
Catalog Number
AA3A75035
Company Name
HYHTE HOLDINGS, INC.
Labeler DUNS
073029645
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-23
Public Version
3
Public Version Date
2023-05-15
Public Version Status
Update
Public Device Record Key
d1a28b34-eb62-4d71-9cbb-a5c929d9e79b

Device Description

HIGH TOP FULL CORTICAL LARGE DIAMETER POLYAXIAL SCREW

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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation
OSH Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis

GMDN Terms

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

Identifiers

Type ID
Primary 00841379130802

Customer Contacts

Phone
7608148047

Device Sizes

Type Value Unit Text
Length 35 Millimeter
Outer Diameter 7.5 Millimeter