FDA UDI In Commercial Distribution 🇺🇸 United States

McGuff

DI: 06972620114112 · Model: 003200 · BQ PLUS MEDICAL CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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
McGuff
Primary DI
06972620114112
Version / Model
003200
Company Name
BQ PLUS MEDICAL CO., LTD.
Labeler DUNS
544463583
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-30
Public Version
1
Public Version Date
2026-04-07
Public Version Status
New
Public Device Record Key
2c66bb64-f0b0-417f-ad84-395a15e558fe

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPA Set, Administration, Intravascular

GMDN Terms

Code Name
58977 Basic intravenous administration set, noninvasive

Identifiers

Type ID
Package 16972620114102
Primary 06972620114112