FDA UDI In Commercial Distribution 🇺🇸 United States

Hetaida

DI: 06970289035649 · Model: K5102US · Hetaida Technology 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
Hetaida
Primary DI
06970289035649
Version / Model
K5102US
Company Name
Hetaida Technology Co., Ltd
Labeler DUNS
544474402
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-14
Public Version
1
Public Version Date
2024-03-22
Public Version Status
New
Public Device Record Key
5ae4dd10-29b5-4e34-a782-1cf077163215

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
INB Attachment, Commode, Wheelchair

GMDN Terms

Code Name
32616 Vaginal douche, reusable

Identifiers

Type ID
Package 16970289035646
Primary 06970289035649

Customer Contacts