FDA UDI In Commercial Distribution 🇺🇸 United States

Elite Medtek

DI: 06939147402030 · Model: EM-ID-M30S · Elite Medtek (Jiangsu) Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Elite Medtek
Primary DI
06939147402030
Version / Model
EM-ID-M30S
Company Name
Elite Medtek (Jiangsu) Co., Ltd.
Labeler DUNS
542974341
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-12
Public Version
1
Public Version Date
2020-08-20
Public Version Status
New
Public Device Record Key
b530e57c-ac6f-4dad-912f-7d86e0a4a27c

Device Characteristics

Single Use
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
PTM Syringe, Balloon Inflation, Exempt

GMDN Terms

Code Name
17541 Catheter/overtube balloon inflator, single-use

Identifiers

Type ID
Primary 06939147402030