FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 04961333248209 · Model: EC38-i10L · HOYA CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
04961333248209
Version / Model
EC38-i10L
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
1
Public Version Date
2020-12-22
Public Version Status
New
Public Device Record Key
0e6652b3-6b94-40c3-83aa-0aa86001edb6

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
FDF Colonoscope and accessories, flexible/rigid

GMDN Terms

Code Name
36117 Flexible video colonoscope, reusable

Identifiers

Type ID
Direct Marking 04961333248186
Primary 04961333248209

Premarket Submissions

Submission Number Supplement Number
K131855 000