FDA UDI In Commercial Distribution 🇺🇸 United States

PULSAR

DI: 04048551242513 · Model: 40160120 · Karl Storz GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PULSAR
Primary DI
04048551242513
Version / Model
40160120
Company Name
Karl Storz GmbH & Co. KG
Labeler DUNS
315731430
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-23
Public Version
1
Public Version Date
2019-03-11
Public Version Status
New
Public Device Record Key
a3132b38-42fa-4553-b22b-5caf4ed1fd59

Device Description

KARL STORZ PULSAR II Stroboscope

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EQL LARYNGOSTROBOSCOPE

GMDN Terms

Code Name
41585 Laryngostroboscope system

Identifiers

Type ID
Primary 04048551242513