FDA UDI In Commercial Distribution 🇺🇸 United States

TEMPO

DI: 20705032064429 · Model: SRD6817 · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TEMPO
Primary DI
20705032064429
Version / Model
SRD6817
Catalog Number
SRD6817
Company Name
CORDIS CORPORATION
Labeler DUNS
806136177
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-01
Public Version
6
Public Version Date
2022-08-10
Public Version Status
Update
Public Device Record Key
98afa927-f873-4fd4-8c6b-b5d953ad089d

Device Description

5 F TEMPO 0.038 INCHES 100CM RH H1

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Primary 20705032064429

Premarket Submissions

Submission Number Supplement Number
K991673 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damanged
Type
Special Storage Condition, Specify
Special Conditions
To prevent damage to the catheter tip during removal from the package, grasp the hub and withdraw the catheter
Type
Special Storage Condition, Specify
Special Conditions
Exposure to temperatures above 54 degrees C (130 F) may damage the catheter
Type
Special Storage Condition, Specify
Special Conditions
Store in cool, dark, dry place