FDA UDI In Commercial Distribution 🇺🇸 United States

Aero-Med

DI: 10885380184031 · Model: CA36350 · Aero-Med, Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Aero-Med
Primary DI
10885380184031
Version / Model
CA36350
Catalog Number
CA36350
Company Name
Aero-Med, Ltd.
Labeler DUNS
194550042
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-23
Public Version
4
Public Version Date
2022-04-08
Public Version Status
Update
Public Device Record Key
290c3269-43c5-4886-8967-86d90bcefc01

Device Description

COVID-19 Collection Kit Kingman Reg

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
OIB Blood and urine collection kit (excludes HIV testing)

GMDN Terms

Code Name
62773 General specimen collection kit IVD, clinical

Identifiers

Type ID
Package 50885380184039
Primary 10885380184031

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius