FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20613994802495 · Model: PSP1000 · MEDTRONIC XOMED, INC.
Product Codes
6
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
20613994802495
Version / Model
PSP1000
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-04-30
Public Version
5
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
f1ba2436-8f34-4343-bba2-184de63803b6

Device Description

PROBE PSP1000 10PK 100MM PEDI SCREW ROHS

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
GWQ Full-montage Standard Electroencephalograph
ITX Transducer, ultrasonic, diagnostic
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE
GWJ STIMULATOR, AUDITORY, EVOKED RESPONSE
GWE STIMULATOR, PHOTIC, EVOKED RESPONSE
IYN System, imaging, pulsed doppler, ultrasonic

GMDN Terms

Code Name
35723 Nerve-locating system

Identifiers

Type ID
Primary 20613994802495
Unit of Use 00613994802491

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K061639 000