Identity
- Trade Name
- TAUB - Trident - IMPULSE FDA UDI
- Generic Name
- Dental prosthesis removal instrument FDA UDI
- Device Name
- IMPULSE is a hand held and operated crown remover. It is a spring loaded device with 3 power settings. Two different tips are provided: A chisel tip for removing cemented crowns off a tooth or implant abutment, A pointed tip for removing cemented bridges, splints, and crowns. The IMPULSE provides a shock "Pulse" to the restoration to break the seal of the cement and allows the restoration to be removed with certain cements. FDA UDI
- Model / Reference
- Crown & Bridge Remover - Polished FDA UDI
- Description
- IMPULSE is a hand held and operated crown remover. It is a spring loaded device with 3 power settings. Two different tips are provided: A chisel tip for removing cemented crowns off a tooth or implant abutment, A pointed tip for removing cemented bridges, splints, and crowns. The IMPULSE provides a shock "Pulse" to the restoration to break the seal of the cement and allows the restoration to be removed with certain cements. FDA UDI
Identifiers
- Catalog Number
- 99-1035 FDA UDI
- Primary DI / UDI-DI
- D8379910350 FDA UDI
- FDA Product Code
- EIS FDA UDI
- GMDN Term
- Dental prosthesis removal instrument FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dental prosthesis removal instrument
TAUB - Trident - IMPULSE by Taub Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental prosthesis removal instrument.
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- devemed — devemed GmbH · Class I
- STOMA® — Storz am Mark 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 | Class I | Pending data |
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Manufacturer
- Manufacturer
- Taub Products
Sources (1)
- FDA UDI b26857c3-48ad-4d12-9992-b51009f1de2d 35 fields · synced May 30, 2026