FDA UDI In Commercial Distribution 🇺🇸 United States

PENTAX

DI: 04961333227686 · Model: VSB-3430K · HOYA CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PENTAX
Primary DI
04961333227686
Version / Model
VSB-3430K
Company Name
HOYA CORPORATION
Labeler DUNS
691519705
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-07
Public Version
4
Public Version Date
2019-02-21
Public Version Status
Update
Public Device Record Key
993fe13d-f247-4131-8669-e020bf372bd1

Device Description

Perform cleaning, high-level disinfection, and/or sterilization according to the procedure specified in the Instructions for Use (Reprocessing) of this instrument.

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
["High-level Disinfectant", "Ethylene Oxide"]

Product Codes

Code Name
FDS Gastroscope and accessories, flexible/rigid

GMDN Terms

Code Name
36299 Flexible video enteroscope

Identifiers

Type ID
Primary 04961333227686

Premarket Submissions

Submission Number Supplement Number
K962897 000