FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10810050244234 · Model: CFI-792 · DOMICO MED-DEVICE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
NA
Primary DI
10810050244234
Version / Model
CFI-792
Company Name
DOMICO MED-DEVICE, LLC
Labeler DUNS
081253414
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2021-04-28
Public Version
1
Public Version Date
2021-05-06
Public Version Status
New
Public Device Record Key
4aae4526-5bf0-43fb-b027-2c2a07fd3425

Device Description

HOLDER, 4 HOLE TEST TUBE

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use

GMDN Terms

Code Name
15186 Test tube rack

Identifiers

Type ID
Unit of Use 00810050244237
Primary 10810050244234