FDA UDI In Commercial Distribution 🇺🇸 United States

Dannik

DI: 10850013527042 · Model: DMP5920 · Dannik LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Dannik
Primary DI
10850013527042
Version / Model
DMP5920
Company Name
Dannik LLC
Labeler DUNS
117407001
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2023-01-21
Public Version
1
Public Version Date
2023-01-30
Public Version Status
New
Public Device Record Key
6e82e278-c0cb-4124-afef-abf6836a73dd

Device Description

Disposable Monopolar 5mm x 33cm Autraumatic Fenestrated Grasper, Ratcheting

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
No
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
58039 Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Unit of Use 00850013527045
Primary 10850013527042

Premarket Submissions

Submission Number Supplement Number
K193019 000