FDA UDI In Commercial Distribution 🇺🇸 United States

Remel

DI: 00848838058271 · Model: R8311008 · REMEL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Remel
Primary DI
00848838058271
Version / Model
R8311008
Company Name
REMEL, INC.
Labeler DUNS
065769564
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2021-11-13
Public Version
2
Public Version Date
2021-12-08
Public Version Status
Update
Public Device Record Key
b6d1ab79-a0a0-459f-98c2-2af09f3a0b30

Device Description

RapID CB PLUS System 20/KT

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
JTO Discs, Strips And Reagents, Microorganism Differentiation

GMDN Terms

Code Name
50419 Multiple aerobic gram positive bacteria species culture isolate identification IVD, kit

Identifiers

Type ID
Unit of Use 30848838058272
Primary 00848838058271

Customer Contacts

Phone
8002556730