FDA UDI In Commercial Distribution 🇺🇸 United States

FibriJet

DI: 00815634021785 · Model: SA-6030 · Micromedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
FibriJet
Primary DI
00815634021785
Version / Model
SA-6030
Company Name
Micromedics, Inc.
Labeler DUNS
066839630
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-21
Public Version
2
Public Version Date
2023-04-25
Public Version Status
Update
Public Device Record Key
4a54f799-6559-48eb-b065-010b25efd6ab

Device Description

FIBRIJET REGULATOR

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CAN Regulator, Pressure, Gas Cylinder

GMDN Terms

Code Name
47860 Surgical air pipeline regulator

Identifiers

Type ID
Package 10815634021782
Primary 00815634021785