Identity
- Trade Name
- MicroAire® FDA UDI
- Generic Name
- Surgical saw blade, oscillating, single-use FDA UDI
- Device Name
- OSCILLATING SAW BLADE, 9.0mm x 31.0mm x 0.51mm FDA UDI
- Model / Reference
- SP-519A FDA UDI
- Description
- OSCILLATING SAW BLADE, 9.0mm x 31.0mm x 0.51mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00847399011701 FDA UDI
- FDA Product Code
- GES FDA UDI
- GMDN Term
- Surgical saw blade, oscillating, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Width — 9 Millimeter FDA UDILength — 31 Millimeter FDA UDI
MicroAire® by MicroAire Surgical Instruments LLC — 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
- MicroAire Surgical Instruments LLC
Sources (1)
- FDA UDI e73ba091-cb43-4875-b187-aed8eb48ae4a 35 fields · synced Jun 9, 2026