FDA UDI In Commercial Distribution 🇺🇸 United States

OMNIBotics

DI: 00841690195320 · Model: XK-06449 · Omni Life Science, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OMNIBotics
Primary DI
00841690195320
Version / Model
XK-06449
Catalog Number
XK-06449
Company Name
Omni Life Science, Inc.
Labeler DUNS
061339651
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-10
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
c29e836e-729d-497f-95b6-5d2fd324c23f

Device Description

iBlock Sawing Guide with Cutout

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 00841690195320

Customer Contacts