FDA UDI In Commercial Distribution 🇺🇸 United States

Orfit

DI: 05401172040385 · Model: 32317/31 · Orfit Industries NV
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Orfit
Primary DI
05401172040385
Version / Model
32317/31
Company Name
Orfit Industries NV
Labeler DUNS
283679900
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-15
Public Version
1
Public Version Date
2026-04-23
Public Version Status
New
Public Device Record Key
1121b9ec-be6c-4fc5-a94a-d81db8cbdaea

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
IYE Accelerator, linear, medical

GMDN Terms

Code Name
61129 Patient positioner base plate

Identifiers

Type ID
Primary 05401172040385

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K991319 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
50 – 96 Degrees Fahrenheit