Identity
- Trade Name
- Hemoban® Gel FDA UDI
- Generic Name
- Dental material injection cannula, single-use FDA UDI
- Device Name
- Hemoban® Gel Infusor Tip Refill FDA UDI
- Model / Reference
- 675120 FDA UDI
- Description
- Hemoban® Gel Infusor Tip Refill FDA UDI
Identifiers
- Catalog Number
- 675120 FDA UDI
- Primary DI / UDI-DI
- D0026751201 FDA UDI
- FDA Product Code
- MVL FDA UDI
- GMDN Term
- Dental material injection cannula, single-use FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental material injection cannula, single-use
Hemoban® Gel by Dentsply International — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class U | Pending data |
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Manufacturer
- Manufacturer
- Dentsply International
Sources (1)
- FDA UDI 2e1de460-36d3-4919-b6bc-a88b95135ac5 36 fields · synced May 30, 2026