FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10705034789552 · Model: 498.220 · Synthes GmbH
Product Codes
5
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034789552
Version / Model
498.220
Catalog Number
498220
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
3
Public Version Date
2022-04-27
Public Version Status
Update
Public Device Record Key
cfba17f5-3c29-4c65-891e-fd06250d529a

Device Description

TI TRANSVERSE BAR 20MM

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

GMDN Terms

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

Identifiers

Type ID
Secondary H9814982200
Primary 10705034789552

Customer Contacts