FDA UDI In Commercial Distribution 🇺🇸 United States

Gimmi

DI: 04049047127086 · Model: E.8000.00 · Gimmi GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Gimmi
Primary DI
04049047127086
Version / Model
E.8000.00
Catalog Number
E.8000.00
Company Name
Gimmi GmbH
Labeler DUNS
316152610
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-05
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
d3b059c8-4ce2-4393-9753-85f634460cae

Device Description

OPTIC LIGHT CABLE TESTER

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
35507 Fibreoptic light cable

Identifiers

Type ID
Primary 04049047127086

Customer Contacts