FDA UDI In Commercial Distribution 🇺🇸 United States

REMEL

DI: 00848838022302 · Model: R21076 · REMEL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REMEL
Primary DI
00848838022302
Version / Model
R21076
Catalog Number
R21076
Company Name
REMEL, INC.
Labeler DUNS
065769564
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-04
Public Version
1
Public Version Date
2023-01-12
Public Version Status
New
Public Device Record Key
1ca76920-a037-4ca9-99e1-51ceb50b3ad7

Device Description

NAC 50 (50ml) PK/6ampules

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
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
LIB Device, General Purpose, Microbiology, Diagnostic

GMDN Terms

Code Name
62707 Culture medium base ingredient IVD

Identifiers

Type ID
Primary 00848838022302