FDA UDI In Commercial Distribution 🇺🇸 United States

PENTAX

DI: 14961333079343 · Model: OF-B173 · HOYA CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
PENTAX
Primary DI
14961333079343
Version / Model
OF-B173
Company Name
HOYA CORPORATION
Labeler DUNS
691519705
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2023-07-31
Public Version
1
Public Version Date
2023-08-08
Public Version Status
New
Public Device Record Key
5a973716-738f-4b96-8145-7f09d2930e1d

Device Description

Rubber Inlet Seal OF-B173

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
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", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
FDS Gastroscope And Accessories, Flexible/Rigid

GMDN Terms

Code Name
60650 Endoscope working-channel seal

Identifiers

Type ID
Unit of Use 04961333079346
Primary 14961333079343

Premarket Submissions

Submission Number Supplement Number
K961564 000