FDA UDI In Commercial Distribution 🇺🇸 United States

Laparoscope

DI: 04059082032269 · Model: 162 104 503 · SOPRO-COMEG GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Laparoscope
Primary DI
04059082032269
Version / Model
162 104 503
Company Name
SOPRO-COMEG GmbH
Labeler DUNS
507185952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-20
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
bbe83044-d39a-4a47-81b8-c212cf33b34c

Device Characteristics

Single Use
No
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
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
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
GCJ Laparoscope, general & plastic surgery

GMDN Terms

Code Name
12291 Rigid optical laparoscope

Identifiers

Type ID
Primary 04059082032269

Premarket Submissions

Submission Number Supplement Number
K945266 000