FDA UDI Not in Commercial Distribution 🇺🇸 United States

USS

DI: 10705034794440 · Model: 499.641 · SYNTHES (U.S.A.) LP
Product Codes
5
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
USS
Primary DI
10705034794440
Version / Model
499.641
Catalog Number
499641
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
4
Public Version Date
2019-06-21
Public Version Status
Update
Public Device Record Key
a0db78ac-3d16-45eb-9550-46e06113cd6f
Distribution End Date
2019-06-21

Device Description

4.2MM TI USS VARIABLE AXIS SCREW 30MM THREAD LENGTH

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
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

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

Identifiers

Type ID
Secondary H9814996410
Primary 10705034794440

Customer Contacts