FDA UDI In Commercial Distribution 🇺🇸 United States

General Instrument

DI: 00841132125489 · Model: 01-1003-6155 · ORTHOPEDIATRICS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
General Instrument
Primary DI
00841132125489
Version / Model
01-1003-6155
Catalog Number
01-1003-6155
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
92e930a0-54ff-4e89-a350-2cba1e5e9d09

Device Description

Hook Trial, Laminar Wide Blade

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
KIK HOOK, BONE

GMDN Terms

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

Identifiers

Type ID
Primary 00841132125489

Customer Contacts