FDA UDI In Commercial Distribution 🇺🇸 United States

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DI: 00841668144657 · Model: 60-5001 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BLINK
Primary DI
00841668144657
Version / Model
60-5001
Catalog Number
60-5001
Company Name
KATENA PRODUCTS, INC.
Labeler DUNS
085668598
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-26
Public Version
1
Public Version Date
2026-04-03
Public Version Status
New
Public Device Record Key
e3ad4229-2cca-4abe-aaf3-58b45c9ec14a

Device Description

Peri/Retrobulbar Needle - 23G23G x 1 1/4", (0.64 x 0.32mm), Atkinson

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
GAA NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE

GMDN Terms

Code Name
47610 Ophthalmic needle, single-use

Identifiers

Type ID
Package 00841668146064
Primary 00841668144657