FDA UDI In Commercial Distribution 🇺🇸 United States

RTK10358 Room Turn Over Kit

DI: 00787551037005 · Model: RTK10358 · XODUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
RTK10358 Room Turn Over Kit
Primary DI
00787551037005
Version / Model
RTK10358
Catalog Number
RTK10358
Company Name
XODUS MEDICAL, INC.
Labeler DUNS
868042664
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
c3e4c6c8-d13a-4305-a3a0-8fc1ded91aab

Device Description

RTK10358 Room Turn Over Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
KDD Kit, surgical instrument, disposable

GMDN Terms

Code Name
65175 Operating room turnover kit

Identifiers

Type ID
Package 20787551037009
Primary 00787551037005

Customer Contacts