FDA UDI In Commercial Distribution 🇺🇸 United States

Ophthalmic Retractor

DI: 00841668100950 · Model: K1-8200 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ophthalmic Retractor
Primary DI
00841668100950
Version / Model
K1-8200
Catalog Number
K1-8200
Company Name
KATENA PRODUCTS, INC.
Labeler DUNS
085668598
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-14
Public Version
2
Public Version Date
2022-12-15
Public Version Status
Update
Public Device Record Key
e3cc5748-26a1-4d5c-b0ab-a1410509f804

Device Description

DESMARRES LID RETRACTOR #0

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HNI Retractor, ophthalmic

GMDN Terms

Code Name
35314 Periocular/lacrimal retractor, hand-held, reusable

Identifiers

Type ID
Primary 00841668100950

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Size 0
Width 11 Millimeter