FDA UDI In Commercial Distribution 🇺🇸 United States

ASEPT

DI: 00813623017023 · Model: M7002 · PFM MEDICAL INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ASEPT
Primary DI
00813623017023
Version / Model
M7002
Catalog Number
M7002
Company Name
PFM MEDICAL INCORPORATED
Labeler DUNS
097736867
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-05
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
7c975506-123f-4075-8125-57fc15f39671

Device Description

ASEPT 600mL Drainage Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
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
KDQ Bottle, Collection, Vacuum

GMDN Terms

Code Name
45391 Closed-wound drainage reservoir suction bulb

Identifiers

Type ID
Package 10813623017020
Primary 00813623017023

Customer Contacts

Phone
7607588749