FDA UDI In Commercial Distribution 🇺🇸 United States

Para-Pak Direct Detect

DI: 00840733103438 · Model: 990125 · MERIDIAN BIOSCIENCE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Para-Pak Direct Detect
Primary DI
00840733103438
Version / Model
990125
Catalog Number
990125
Company Name
MERIDIAN BIOSCIENCE, INC.
Labeler DUNS
092815364
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-07
Public Version
1
Public Version Date
2021-07-15
Public Version Status
New
Public Device Record Key
7d356cea-f674-4ad8-97a7-4deaa3b1dda7

Device Description

This UDI represents the inner pack configuration for the Para-Pak Direct Detect product. The inner pack consists of one vial per bag. The Direct Detect is a disposable specimen collection device. Clean vial in a transport bag.

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
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
No
Sterilization Prior Use
No

Product Codes

Code Name
FMH Container, Specimen, Sterile

GMDN Terms

Code Name
57907 Faecal specimen container IVD, no additive

Identifiers

Type ID
Primary 00840733103438

Customer Contacts

Phone
800-343-3858

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius