FDA UDI In Commercial Distribution 🇺🇸 United States

Skytron

DI: 10841736116705 · Model: 4-031-01 · SKYTRON LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Skytron
Primary DI
10841736116705
Version / Model
4-031-01
Catalog Number
4-031-01
Company Name
SKYTRON LLC
Labeler DUNS
078375583
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-29
Public Version
1
Public Version Date
2022-02-07
Public Version Status
New
Public Device Record Key
932a9e99-587c-407a-b03a-43592d3d0e01

Device Description

44 Inch Carbon Fiber Extension G-Series

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
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
FQO TABLE, OPERATING-ROOM, AC-POWERED

GMDN Terms

Code Name
61131 Radiological general body-part positioner

Identifiers

Type ID
Primary 10841736116705

Customer Contacts

Device Sizes

Type Value Unit Text
Length 44 Inch

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity