FDA UDI In Commercial Distribution 🇺🇸 United States

DISP PERIBULBAR NEDLE 23GA 1 1/4" 10/BOX

DI: 00841668111932 · Model: AS-7069 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
DISP PERIBULBAR NEDLE 23GA 1 1/4" 10/BOX
Primary DI
00841668111932
Version / Model
AS-7069
Catalog Number
AS-7069
Company Name
KATENA PRODUCTS, INC.
Labeler DUNS
085668598
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-12-13
Public Version
1
Public Version Date
2022-12-21
Public Version Status
New
Public Device Record Key
b21fed47-b000-4e45-98db-77015e697855

Device Description

DISP PERIBULBAR NEDLE 23GA 1 1/4" 10/BOX

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
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
No

Product Codes

Code Name
HMX Cannula, ophthalmic

GMDN Terms

Code Name
46705 Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

Identifiers

Type ID
Unit of Use 10841668111939
Primary 00841668111932

Customer Contacts

Device Sizes

Type Value Unit Text
Needle Gauge 23 Gauge