FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00840682138130 · Model: 5432778 · USA INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00840682138130
Version / Model
5432778
Company Name
USA INSTRUMENTS, INC.
Labeler DUNS
804517571
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-08
Public Version
5
Public Version Date
2019-05-23
Public Version Status
Update
Public Device Record Key
adf04ebc-aa09-4f5e-acc4-68706cc1b045

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KXH Cradle, patient, radiologic

GMDN Terms

Code Name
40902 Radiological whole-body positioner

Identifiers

Type ID
Primary 00840682138130

Premarket Submissions

Submission Number Supplement Number
K122174 000