FDA UDI In Commercial Distribution 🇺🇸 United States

LASS

DI: 00853714008059 · Model: LP1001 · RADUX DEVICES, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LASS
Primary DI
00853714008059
Version / Model
LP1001
Catalog Number
LP1001
Company Name
RADUX DEVICES, LLC
Labeler DUNS
079668796
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-31
Public Version
1
Public Version Date
2024-02-08
Public Version Status
New
Public Device Record Key
cc808cdd-5a53-404a-98af-1965b58e43b5

Device Description

LASS Base Board

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
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
CCX Support, Patient Position

GMDN Terms

Code Name
65180 Operating table patient positioning set, reusable

Identifiers

Type ID
Primary 00853714008059

Customer Contacts

Phone
800-935-3137