Identity
- Trade Name
- Select Bioclear Evolve Posterior Kit FDA UDI
- Generic Name
- Dental matrix band kit FDA UDI
- Device Name
- Convenience kit of Bioclear products used in posterior dental restorations. FDA UDI
- Model / Reference
- Select FDA UDI
- Description
- Convenience kit of Bioclear products used in posterior dental restorations. FDA UDI
Identifiers
- Primary DI / UDI-DI
- D9498271312 FDA UDI
- GMDN Term
- Dental matrix band kit FDA UDI
Classification
- Commercial Distribution
- 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
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dressing/utility forceps, scissors-like, reusableDental implantation depth/angle gauge, reusableManual non-rotary dental instrument handleDental wedge, single-use
Select Bioclear Evolve Posterior Kit by Bioclear Matrix Systems, LLC — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental matrix band retainer.
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- Reicodent — devemed GmbH · Class I
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Bioclear Matrix Systems, LLC
Sources (1)
- FDA UDI 582b45bc-74ee-47d7-949c-1e93d2500a10 33 fields · synced May 30, 2026