FDA UDI In Commercial Distribution 🇺🇸 United States

Ophthlamic Speculum

DI: 10841668115159 · Model: K20-1007 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Ophthlamic Speculum
Primary DI
10841668115159
Version / Model
K20-1007
Catalog Number
K20-1007
Company Name
KATENA PRODUCTS, INC.
Labeler DUNS
085668598
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
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
556e90b8-89e2-4123-9671-0837b9f98205

Device Description

BARRAQUER SPECULUM Disposable with Finger tabs BOX OF 10

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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
HNC Specula, ophthalmic

GMDN Terms

Code Name
46959 Eyelid speculum, single-use

Identifiers

Type ID
Unit of Use 00841668115152
Primary 10841668115159

Customer Contacts