FDA UDI In Commercial Distribution 🇺🇸 United States

VIDEO ESOPHAGOSCOPE

DI: 04961333232437 · Model: EE-1580K · PENTAX OF AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VIDEO ESOPHAGOSCOPE
Primary DI
04961333232437
Version / Model
EE-1580K
Company Name
PENTAX OF AMERICA, INC.
Labeler DUNS
083211284
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-06
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
8d8ea4b6-740e-4ade-ae88-526903f3ff64

Device Description

VIDEO ESOPHAGOSCOPE (REFURBISHED)

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Ethylene Oxide", "High-level Disinfectant"]

Product Codes

Code Name
FDS Gastroscope And Accessories, Flexible/Rigid

GMDN Terms

Code Name
38666 Flexible video oesophagoscope, reusable

Identifiers

Type ID
Primary 04961333232437

Premarket Submissions

Submission Number Supplement Number
K961564 000