FDA UDI In Commercial Distribution 🇺🇸 United States

3.6V PROFESSIONAL SPOT RET & CASE

DI: 05055272701587 · Model: 1302-P-1009 · KEELER LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
3.6V PROFESSIONAL SPOT RET & CASE
Primary DI
05055272701587
Version / Model
1302-P-1009
Company Name
KEELER LIMITED
Labeler DUNS
210164398
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-26
Public Version
4
Public Version Date
2023-02-06
Public Version Status
Update
Public Device Record Key
c8882ba9-ced8-4dc3-aabb-17e2580cf741

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HKL Retinoscope, Ac-Powered

GMDN Terms

Code Name
46784 Retinoscope, line-powered

Identifiers

Type ID
Primary 05055272701587