FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 08809319842835 · Model: 730-20012 · TDM Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
08809319842835
Version / Model
730-20012
Catalog Number
730-20012
Company Name
TDM Co., Ltd.
Labeler DUNS
557801921
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-07
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
8e62e58f-2b32-4765-968e-3ed9665ca55c

Device Description

3.0/4.0mm HCC Screw 12mm

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
Yes
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
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 08809319842835

Premarket Submissions

Submission Number Supplement Number
K190830 000

Device Sizes

Type Value Unit Text
Outer Diameter 3.3 Millimeter
Length 12 Millimeter