FDA UDI In Commercial Distribution 🇺🇸 United States

Neotech Ocular Exam Kit

DI: 10812594012492 · Model: Standard · Neotech Products LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Neotech Ocular Exam Kit
Primary DI
10812594012492
Version / Model
Standard
Catalog Number
N6511
Company Name
Neotech Products LLC
Labeler DUNS
198013435
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2021-06-14
Public Version
3
Public Version Date
2023-09-21
Public Version Status
Update
Public Device Record Key
6815a113-9754-4f50-b6ef-5ee4e4a86b7b

Device Description

The Neotech Ocular Exam Kit is intended to assist in ocular examinations.

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
High-level Disinfectant

Product Codes

Code Name
FXG Specula Accessories

GMDN Terms

Code Name
46959 Eyelid speculum, single-use

Identifiers

Type ID
Unit of Use 00812594012495
Primary 10812594012492