FDA UDI In Commercial Distribution 🇺🇸 United States

Ref-Keratometer ERK-9100

DI: 08800019600503 · Model: ERK-9100 · Huvitz Co., Ltd.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ref-Keratometer ERK-9100
Primary DI
08800019600503
Version / Model
ERK-9100
Catalog Number
ERK-9100
Company Name
Huvitz Co., Ltd.
Labeler DUNS
688154202
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-12
Public Version
1
Public Version Date
2023-06-20
Public Version Status
New
Public Device Record Key
154eaeec-1d50-4b94-89f4-a83c17bbc896

Device Description

Ref-Keratometer ERK-9100

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
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
No

Product Codes

Code Name
HKO Refractometer, Ophthalmic

GMDN Terms

Code Name
36386 Automated ophthalmic refractometer
12811 Bench-top keratometer

Identifiers

Type ID
Primary 08800019600503

Customer Contacts

Phone
+82314289100