FDA UDI Not in Commercial Distribution 🇺🇸 United States

5391

DI: 00643169382978 · Model: 5391 · Oscor Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
5391
Primary DI
00643169382978
Version / Model
5391
Catalog Number
5391
Company Name
Oscor Inc.
Labeler DUNS
101835833
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
5
Public Version Date
2021-09-10
Public Version Status
Update
Public Device Record Key
f6f3a52f-f7ee-4575-bdd4-d943ce496f04
Distribution End Date
2017-04-13

Device Description

Single Chamber External Pacemaker

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
DTE PULSE-GENERATOR, PACEMAKER, EXTERNAL

GMDN Terms

Code Name
35224 External pacemaker, epicardial pacing

Identifiers

Type ID
Primary 00643169382978

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K033130 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius