FDA UDI In Commercial Distribution 🇺🇸 United States

BDT2.0L22

DI: 03700569601386 · Model: BDT2.0L22 · NEWCLIP TECHNICS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BDT2.0L22
Primary DI
03700569601386
Version / Model
BDT2.0L22
Catalog Number
BDT2.0L22
Company Name
NEWCLIP TECHNICS
Labeler DUNS
263281904
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-10
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
ee2f3ea7-90b0-407c-a11b-8b35ba1582f7

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 03700569601386

Premarket Submissions

Submission Number Supplement Number
K061917 000