Identity
- Trade Name
- Electric System 6 Stryker Precision FDA UDI
- Generic Name
- Bone/joint surgical power tool motorized handpiece/set, electric, reusable FDA UDI
- Device Name
- Oscillating Tip Saw FDA UDI
- Model / Reference
- 6299000000 FDA UDI
- Description
- Oscillating Tip Saw FDA UDI
Identifiers
- Catalog Number
- 6299-000-000 FDA UDI
- Primary DI / UDI-DI
- 07613154501410 FDA UDI
- FDA Product Code
- HWE FDA UDI
- GMDN Term
- Bone/joint surgical power tool motorized handpiece/set, electric, 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone/joint surgical power tool motorized handpiece/set, electric, reusable
Electric System 6 Stryker Precision by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone/joint surgical power tool motorized handpiece/set, electric, reusable.
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC. · Class I
- SSG10 — Saeshin Precision Co., Ltd. · Class II
- Arthrex® — Arthrex, Inc. · Class I
- De Soutter Medical — De Soutter Medical, Ltd. · Class I
- Arthrex® — Arthrex, Inc. · Class I
- ACCULAN 3TI — AESCULAP, 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 42c3a17a-322b-42a3-b71f-90914accc8b6 36 fields · synced Jun 1, 2026