Identity
- Trade Name
- Expasyl FDA UDI
- Generic Name
- Dental material injection cannula, single-use FDA UDI
- Device Name
- Temporary Gingival Retraction System - 100 Applicator Tips FDA UDI
- Model / Reference
- 32264 FDA UDI
- Description
- Temporary Gingival Retraction System - 100 Applicator Tips FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10841396117067 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
Yes
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dental material injection cannula, single-use
Expasyl by Kerr Corporation — 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
- Kerr Corporation
Sources (1)
- FDA UDI 1512f3cc-f074-4dec-a0e4-a67b86ac3eb4 34 fields · synced Jun 8, 2026