FDA UDI In Commercial Distribution 🇺🇸 United States

Uvision Hysteroscope

DI: 00853277008015 · Model: LUMDTx-A1 · UVISION 360, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Uvision Hysteroscope
Primary DI
00853277008015
Version / Model
LUMDTx-A1
Catalog Number
20010
Company Name
UVISION 360, INC.
Labeler DUNS
080826327
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-30
Public Version
2
Public Version Date
2019-11-05
Public Version Status
Update
Public Device Record Key
f21ab7a4-c71a-4142-94d5-078d6b86b3d6

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
Yes
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
Yes
Sterilization Methods
High-level Disinfectant

Product Codes

Code Name
HIH Hysteroscope (And Accessories)
FAJ Cystoscope And Accessories, Flexible/Rigid

GMDN Terms

Code Name
63564 Endoscope sheath, single-use

Identifiers

Type ID
Primary 00853277008015

Premarket Submissions

Submission Number Supplement Number
K181909 000