FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00643169071827 · Model: 945ITP916 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
N/A
Primary DI
00643169071827
Version / Model
945ITP916
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-13
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
da00ab60-9cf3-479f-8ac2-f11304ac648d

Device Description

CONNECTOR 945ITP916 IMPED TEST

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
No
Sterilization Prior Use
No

Product Codes

Code Name
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE

GMDN Terms

Code Name
35723 Nerve-locating system

Identifiers

Type ID
Primary 00643169071827

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K050798 000