FDA UDI In Commercial Distribution 🇺🇸 United States

Manifold Set

DI: 10816203021950 · Model: SDv-9M141 · ORIGEN BIOMEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Manifold Set
Primary DI
10816203021950
Version / Model
SDv-9M141
Company Name
ORIGEN BIOMEDICAL, INC.
Labeler DUNS
625272232
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
170f7426-4a3b-4580-a194-dc562285164c

Device Description

One spike, vented drip chamber to 9 male luers w/140cm SCD tubing, pinch clamps

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
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
KJG Tube, Tissue Culture

GMDN Terms

Code Name
43324 Fluid transfer set, general-purpose

Identifiers

Type ID
Primary 10816203021950
Package 20816203021957

Customer Contacts

Phone
512-474-7278