FDA UDI Not in Commercial Distribution 🇺🇸 United States

Pulset

DI: 00709078007347 · Model: 3372-95 · WESTMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pulset
Primary DI
00709078007347
Version / Model
3372-95
Company Name
WESTMED, INC.
Labeler DUNS
092673953
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-31
Public Version
3
Public Version Date
2022-09-30
Public Version Status
Update
Public Device Record Key
1a99ee1e-255b-42d2-91ee-3c5e9a575b53
Distribution End Date
2022-09-30

Device Description

Full Kit, Pulset 3cc Syringe 22g x 1" (.7 x 25mm) Crickett 25u Balanced Heparin

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
CBT Arterial Blood Sampling Kit

GMDN Terms

Code Name
31336 Arterial blood sampling kit

Identifiers

Type ID
Package 10709078007344
Primary 00709078007347