FDA UDI In Commercial Distribution 🇺🇸 United States

PULSAR®II

DI: 00643169078406 · Model: PS100-100RF · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PULSAR®II
Primary DI
00643169078406
Version / Model
PS100-100RF
Company Name
MEDTRONIC, INC.
Labeler DUNS
030200852
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-16
Public Version
3
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
35a65415-c51a-4053-a2c6-c0ee5a0a017c

Device Description

GENERATOR PS100-100RF REFURB PULSAR

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
11490 Electrosurgical system generator

Identifiers

Type ID
Primary 00643169078406

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 100 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius