Identity
- Trade Name
- KnifeLight FDA UDI
- Generic Name
- Hand ligament surgical release instrument FDA UDI
- Device Name
- KNIFE LIGHT 10,PK FDA UDI
- Model / Reference
- 3300-001-000 FDA UDI
- Description
- KNIFE LIGHT 10,PK FDA UDI
Identifiers
- Catalog Number
- 3300-001-000 FDA UDI
- Primary DI / UDI-DI
- 34546540060113 FDA UDI
- FDA Product Code
- FTD FDA UDI
- GMDN Term
- Hand ligament surgical release instrument FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4580 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Height — 102.0 Millimeter FDA UDIWidth — 292.0 Millimeter FDA UDILength — 305.0 Millimeter FDA UDI
Category: Hand ligament surgical release instrument
KnifeLight by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Hand ligament surgical release instrument.
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
- Stryker Corp.
Sources (1)
- FDA UDI 0309ad11-37f3-465e-a3ff-59540561554e 36 fields · synced Jun 8, 2026