FDA UDI In Commercial Distribution 🇺🇸 United States

Ophthalmic Speculum

DI: 00841668100301 · Model: K1-5330 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ophthalmic Speculum
Primary DI
00841668100301
Version / Model
K1-5330
Catalog Number
K1-5330
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
cf2a79c8-c139-4d2d-90bb-e017c04347a9

Device Description

INFANT WIRE SPECULUM 3MM/5MM BLADES

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
Yes
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
HNC Specula, ophthalmic

GMDN Terms

Code Name
35349 Eyelid speculum, reusable

Identifiers

Type ID
Primary 00841668100301

Customer Contacts