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Externa® Universal Temporary Bioabutment® Ø5 L:3 Mm, Rotating
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- EXTERNA® UNIVERSAL TEMPORARY BIOABUTMENT® Ø5 L:3 MM, ROTATING FDA UDI
- Generic Name
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
- Model / Reference
- CPIUB03 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08435389808114 FDA UDI
- FDA Product Code
- DZE FDA UDI
- GMDN Term
- Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3640 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 5 Millimeter FDA UDILength — 3 Millimeter FDA UDI
Category: Dental implant suprastructure, temporary, preformed, single-use
Externa® Universal Temporary Bioabutment® Ø5 L:3 Mm, Rotating by Biotechnology Institute Sl — Class II — FDA UDI — listed in FDA GUDID
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Also classified as Dental implant suprastructure, temporary, preformed, single-use.
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- Neoss Implant System — Neoss, Ltd. · Class II
- Scanbody Screw — ARUM DENTISTRY Co., Ltd. · 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 | Class II | Pending data |
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Manufacturer
- Manufacturer
- Biotechnology Institute Sl
Sources (1)
- FDA UDI cb405b1f-4138-4684-bfd9-a763895dc63e 34 fields · synced Jun 8, 2026