FDA UDI In Commercial Distribution 🇺🇸 United States

HIPLOC™ SYSTEM

DI: 00887868214844 · Model: 236055 · Biomet Uk Ltd
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HIPLOC™ SYSTEM
Primary DI
00887868214844
Version / Model
236055
Catalog Number
236055
Company Name
Biomet Uk Ltd
Labeler DUNS
219322575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-09
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
05225a69-4fa7-4da3-bc0c-f3d3c41d9a13

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JDO DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 00887868214844

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080685 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Ø12.5 X 55MM