FDA UDI In Commercial Distribution 🇺🇸 United States

General Instrument

DI: 00841132128558 · Model: 03-1008-0013 · ORTHOPEDIATRICS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
General Instrument
Primary DI
00841132128558
Version / Model
03-1008-0013
Catalog Number
03-1008-0013
Company Name
ORTHOPEDIATRICS CORP.
Labeler DUNS
796416191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-25
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
15287cd5-4c60-4762-aaac-318f4fc8e89f

Device Description

Extended Drill Guide Frame

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
No
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
No

Product Codes

Code Name
FZX Guide, surgical, instrument

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 00841132128558

Customer Contacts