FDA UDI In Commercial Distribution 🇺🇸 United States

Ocata Anterior Cervical System

DI: B07308K0120030 · Model: 08-K01-2003 · Kalitec Direct LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ocata Anterior Cervical System
Primary DI
B07308K0120030
Version / Model
08-K01-2003
Company Name
Kalitec Direct LLC
Labeler DUNS
041956211
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-11
Public Version
4
Public Version Date
2019-04-23
Public Version Status
Update
Public Device Record Key
42a271a0-ad59-4617-af99-6bb2615c7d82

Device Description

Removal Sleeve

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
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
HWB Extractor

GMDN Terms

Code Name
12696 Orthopaedic implant inserter/extractor, reusable

Identifiers

Type ID
Primary B07308K0120030