FDA UDI Not in Commercial Distribution 🇺🇸 United States

SURFLASH

DI: 34987350709708 · Model: SR*FVP1832 · TERUMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
SURFLASH
Primary DI
34987350709708
Version / Model
SR*FVP1832
Company Name
TERUMO CORPORATION
Labeler DUNS
690543319
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-09
Public Version
3
Public Version Date
2018-09-14
Public Version Status
Update
Public Device Record Key
d6d98d64-5267-4434-895c-dcaf608023be
Distribution End Date
2018-08-29

Device Description

SURFLASH Plus

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
MR Conditional
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
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days

GMDN Terms

Code Name
40601 Peripheral vascular catheter

Identifiers

Type ID
Package 54987350709702
Primary 34987350709708
Unit of Use 04987350709707

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Catheter Gauge 18 Gauge
Length 1.25 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Stacking limit by 5, Keep away from sunlight, Fragile, handle with care, Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Do not store at extreme temperature and humidity.