FDA UDI In Commercial Distribution 🇺🇸 United States

P-K Titanium Motility Peg System

DI: 00854066006236 · Model: I00057 · INTEGRATED ORBITAL IMPLANTS INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
P-K Titanium Motility Peg System
Primary DI
00854066006236
Version / Model
I00057
Company Name
INTEGRATED ORBITAL IMPLANTS INC
Labeler DUNS
859186348
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-15
Public Version
1
Public Version Date
2024-03-25
Public Version Status
New
Public Device Record Key
965a677f-08ff-4cb4-a667-66c99cba9081

Device Description

Titanium Threaded Sleeve Driver (Wrench) used with IOI's Titanium Threaded Sleeve/Flat Peg (I00045) and Titanium Large Threaded Sleeve/Flat Peg (I00100). Manual, single-use, nonsterile surgical instrument.

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
LRZ Screwdriver, Surgical

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary 00854066006236

Customer Contacts