Identity
- Trade Name
- DT Illusion XRO Intro Kit FDA UDI
- Generic Name
- Root canal post kit FDA UDI
- Model / Reference
- G-91820K FDA UDI
Identifiers
- Catalog Number
- G-91820K FDA UDI
- Primary DI / UDI-DI
- D757G91820K1 FDA UDI
- FDA Product Code
- DZA FDA UDIELR FDA UDI
- GMDN Term
- Root canal post kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4130 FDA UDI872.3810 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
DT Illusion XRO Intro Kit by Bisco Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Bisco Inc.
Sources (1)
- FDA UDI 500090d5-ba26-4266-9f97-cb5c48a7fc72 37 fields · synced Jun 1, 2026