FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 04961333248315 · Model: EG29-i10 · HOYA CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
04961333248315
Version / Model
EG29-i10
Company Name
HOYA CORPORATION
Labeler DUNS
691519705
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-14
Public Version
2
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
60ae8b38-5590-4a95-bd3e-72165a0f9d67

Device Description

Made in Malaysia

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
Yes
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
17663 Flexible video gastroscope, reusable

Identifiers

Type ID
Direct Marking 04961333248292
Primary 04961333248315

Premarket Submissions

Submission Number Supplement Number
K131902 000