FDA UDI In Commercial Distribution 🇺🇸 United States

MurphyScope

DI: 00643169103535 · Model: 2125-163 · MEDTRONIC PS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MurphyScope
Primary DI
00643169103535
Version / Model
2125-163
Company Name
MEDTRONIC PS MEDICAL, INC.
Labeler DUNS
089055867
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-13
Public Version
4
Public Version Date
2023-11-03
Public Version Status
Update
Public Device Record Key
b8fddf0f-8c2e-48aa-94dd-8b0c1dabe37a

Device Description

MURPHYSCOPE 2125-163 MALLE 5 STIP S

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GWG ENDOSCOPE, NEUROLOGICAL

GMDN Terms

Code Name
37181 Flexible fibreoptic intracranial/spinal endoscope

Identifiers

Type ID
Primary 00643169103535

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K010341 000

Device Sizes

Type Value Unit Text
Length 15.0 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry