FDA UDI In Commercial Distribution 🇺🇸 United States

20ga Dex™ Serrated Jaw Forceps

DI: 00817489022009 · Model: DVF4016-20 · KATALYST SURGICAL LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
20ga Dex™ Serrated Jaw Forceps
Primary DI
00817489022009
Version / Model
DVF4016-20
Company Name
KATALYST SURGICAL LLC
Labeler DUNS
007883297
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-11
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
ac48267c-1a23-4f37-a1d4-2cd44ae46114

Device Description

Box of 5, 20ga Dex™ Serrated Jaw Forceps

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HNR Forceps, Ophthalmic

GMDN Terms

Code Name
46710 Ophthalmic tissue forceps, single-use

Identifiers

Type ID
Primary 00817489022009