FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04250869658232 · Model: 113-092-9030 · Biedermann Motech GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04250869658232
Version / Model
113-092-9030
Catalog Number
113-092-9030
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
2021-09-16
Public Version
1
Public Version Date
2021-09-24
Public Version Status
New
Public Device Record Key
c3ac9c96-9ac2-4edf-b036-9bcbd18fa699

Device Description

MOSS XT Ti Pedicle Screw Ø9.0x30mm pink, cannulated DL, polyaxial

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

GMDN Terms

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

Identifiers

Type ID
Primary 04250869658232