FDA UDI Not in Commercial Distribution 🇺🇸 United States

CUSTOM

DI: 03613720283072 · Model: A99191500 · MEDICREA INTERNATIONAL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CUSTOM
Primary DI
03613720283072
Version / Model
A99191500
Catalog Number
A99191500
Company Name
MEDICREA INTERNATIONAL
Labeler DUNS
383228632
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-13
Public Version
4
Public Version Date
2022-12-19
Public Version Status
Update
Public Device Record Key
d28b3743-f5e0-4a4f-9caf-99803ae4eb1b
Distribution End Date
2021-10-04

Device Description

TULIP GENESIS POWER M LOCKING SCREWDRIVER

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
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
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 03613720283072