FDA UDI Not in Commercial Distribution 🇺🇸 United States

Gimmi

DI: 04049047094982 · Model: T.0013.05 · Gimmi GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Gimmi
Primary DI
04049047094982
Version / Model
T.0013.05
Catalog Number
T.0013.05
Company Name
Gimmi GmbH
Labeler DUNS
316152610
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-05
Public Version
4
Public Version Date
2022-04-28
Public Version Status
Update
Public Device Record Key
4d7f3e0c-0487-43a2-997d-e6a6bea58cf5
Distribution End Date
2017-05-06

Device Description

BIPOLAR COAGULATION FORCEPS COMPLETE BIPOLAR COAGULATION FORCEPS COMPLETE Ø 5 MM, FORCEPS 1.5 MM WIDE

Device Characteristics

Single Use
No
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
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
32684 Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

Identifiers

Type ID
Primary 04049047094982

Customer Contacts