Identity
- Trade Name
- QUICK-DIE Refill Package FDA UDI
- Generic Name
- Polymer-based dental model material FDA UDI
- Model / Reference
- L-11090P FDA UDI
Identifiers
- Catalog Number
- L-11090P FDA UDI
- Primary DI / UDI-DI
- D757L11090P1 FDA UDI
- 510(k) Number
- K962680 FDA UDI
- FDA Product Code
- ELW FDA UDI
- GMDN Term
- Polymer-based dental model material FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3660 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
QUICK-DIE Refill Package by Bisco Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
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Manufacturer
- Manufacturer
- Bisco Inc.
Sources (1)
- FDA UDI 60e969a5-27ea-40bb-9a96-7dc21929afa7 38 fields · synced May 29, 2026