FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04250869602914 · Model: 107-017-0001 · Biedermann Motech GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04250869602914
Version / Model
107-017-0001
Catalog Number
107-017-0001
Company Name
Biedermann Motech GmbH & Co. KG
Labeler DUNS
320249162
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-10
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
9a3f41f0-d8f2-4d80-9761-ccfa558aac28

Device Description

MOSS 100 Ti Head, Standard Polyaxial, rod system Ø5.5mm

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 Orthosis, spinal pedicle fixation, for degenerative disc disease

GMDN Terms

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

Identifiers

Type ID
Primary 04250869602914

Premarket Submissions

Submission Number Supplement Number
K162232 000