FDA UDI In Commercial Distribution 🇺🇸 United States

ElevatorMax

DI: S062110000 · Model: Base · Pausch, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ElevatorMax
Primary DI
S062110000
Version / Model
Base
Catalog Number
S 0621 1000
Company Name
Pausch, L.L.C.
Labeler DUNS
080365572
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-24
Public Version
1
Public Version Date
2024-05-02
Public Version Status
New
Public Device Record Key
bc71211d-58f2-4cd4-b631-1aa2593fda35

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IZZ Table, Radiographic, Non-Tilting, Powered

GMDN Terms

Code Name
65313 Diagnostic X-ray system positioning frame

Identifiers

Type ID
Primary S062110000