FDA UDI In Commercial Distribution 🇺🇸 United States

Geminus

DI: 10841506105441 · Model: K-Wire, 2.0mm/1.5mm x 127mm, 316LVM (3 pack) · SKELETAL DYNAMICS L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Geminus
Primary DI
10841506105441
Version / Model
K-Wire, 2.0mm/1.5mm x 127mm, 316LVM (3 pack)
Catalog Number
KWR3-D20-15127
Company Name
SKELETAL DYNAMICS L.L.C.
Labeler DUNS
869056148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-21
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
ba7af083-3e70-4e37-97c4-03cfd6184bb4

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
No

Product Codes

Code Name
HRS Plate, fixation, bone

GMDN Terms

Code Name
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 10841506105441

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111620 000