FDA UDI In Commercial Distribution 🇺🇸 United States

XPLUS 35 Series

DI: 08800098700163 · Model: XPLUS 35 · GEMSS Healthcare Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
XPLUS 35 Series
Primary DI
08800098700163
Version / Model
XPLUS 35
Company Name
GEMSS Healthcare Co., Ltd.
Labeler DUNS
694184465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-16
Public Version
1
Public Version Date
2026-01-26
Public Version Status
New
Public Device Record Key
97e1d33c-52c2-47c7-b2df-3a4379368473

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
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
OWB Interventional Fluoroscopic X-Ray System

GMDN Terms

Code Name
37646 Mobile general-purpose fluoroscopic x-ray system, digital

Identifiers

Type ID
Primary 08800098700163

Premarket Submissions

Submission Number Supplement Number
K233200 000