FDA UDI In Commercial Distribution 🇺🇸 United States

BKG

DI: 00810011730557 · Model: Ordinary Type · Tianjin Huahong Technology Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
BKG
Primary DI
00810011730557
Version / Model
Ordinary Type
Company Name
Tianjin Huahong Technology Co., Ltd.
Labeler DUNS
421272490
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2024-10-24
Public Version
2
Public Version Date
2025-04-25
Public Version Status
Update
Public Device Record Key
912afa7e-4d7b-4c97-b732-3cc17ceeb549

Device Characteristics

Single Use
Yes
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
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
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
44127 Autoinjector needle

Identifiers

Type ID
Package 10810011730554
Primary 00810011730557
Unit of Use 50810011730552