Identity
- Trade Name
- Two Striper FDA UDI
- Generic Name
- Podiatric bur, reusable FDA UDI
- Device Name
- Diamond Podiatry Bur FDA UDI
- Model / Reference
- PODIATRY SYSTEM (4 TOOLS) FDA UDI
- Description
- Diamond Podiatry Bur FDA UDI
Identifiers
- Catalog Number
- CFMDPDKT050 FDA UDI
- Primary DI / UDI-DI
- B868CFMDPDKT0501 FDA UDI
- FDA Product Code
- GFF FDA UDI
- GMDN Term
- Podiatric bur, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
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
Moist Heat or Steam Sterilization FDA UDI
Category: Podiatric bur, reusable
A comprehensive medical device directory for the Two Striper podiatry bur, providing detailed information on its features, compliance, and FAQs.
Similar devices
Also classified as Podiatric bur, reusable.
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
- Abrasive Technology, Llc
Sources (1)
- FDA UDI 82b11fe8-e71f-4996-883c-6b2e37cdd355 34 fields · synced Jul 25, 2026