Identity
- Trade Name
- SGO-1 FDA UDI
- Generic Name
- Surgical saw blade, oscillating, reusable FDA UDI
- Model / Reference
- SGO-1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04560264501423 FDA UDI
- FDA Product Code
- KMW FDA UDI
- GMDN Term
- Surgical saw blade, oscillating, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.4120 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
No
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: Surgical saw blade, oscillating, reusable
Sgo-1 by Nakanishi Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical saw blade, oscillating, reusable.
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- Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
- OSUNG MND — Osung Mnd Co., Ltd. · Class I
- Saw blade 13.3/6.0/0, 4mm — Nouvag AG · Class I
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · 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
- Nakanishi Inc.
Sources (1)
- FDA UDI 0fb8ef0f-3289-4f69-9663-676e3f8e6a2d 32 fields · synced May 30, 2026