FDA UDI In Commercial Distribution 🇺🇸 United States

Balloon Inflation Device

DI: 06936841236329 · Model: BT-30 (25mL) -DG · Tianck Medical Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Balloon Inflation Device
Primary DI
06936841236329
Version / Model
BT-30 (25mL) -DG
Catalog Number
100002
Company Name
Tianck Medical Co., Ltd.
Labeler DUNS
418642903
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-12
Public Version
1
Public Version Date
2025-11-20
Public Version Status
New
Public Device Record Key
ce2d09a9-7ab5-4e62-a880-c4252ef14d78

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
No

Product Codes

Code Name
PTM Syringe, Balloon Inflation, Exempt

GMDN Terms

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

Identifiers

Type ID
Primary 06936841236329