FDA UDI In Commercial Distribution 🇺🇸 United States

PROBST LASIK SPECULUM 10/BOX

DI: 00841668142967 · Model: AS-1008 · KATENA PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
PROBST LASIK SPECULUM 10/BOX
Primary DI
00841668142967
Version / Model
AS-1008
Catalog Number
AS-1008
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
3792aa1c-2014-4ca4-849c-ef9641701c1c

Device Description

PROBST LASIK SPECULUM 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
HNC Specula, ophthalmic

GMDN Terms

Code Name
46959 Eyelid speculum, single-use

Identifiers

Type ID
Unit of Use 10841668142964
Primary 00841668142967

Customer Contacts