FDA UDI In Commercial Distribution 🇺🇸 United States

PENTAX

DI: 04961333233793 · Model: EG-3270UK · HOYA CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PENTAX
Primary DI
04961333233793
Version / Model
EG-3270UK
Company Name
HOYA CORPORATION
Labeler DUNS
691519705
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-10
Public Version
1
Public Version Date
2018-09-10
Public Version Status
New
Public Device Record Key
278cc05a-020f-4e06-a696-9ea176ba2a6a

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
ODG Endoscopic Ultrasound System, Gastroenterology-Urology

GMDN Terms

Code Name
36951 Flexible ultrasound gastroduodenoscope

Identifiers

Type ID
Primary 04961333233793

Premarket Submissions

Submission Number Supplement Number
K162447 000