← Back to catalogue
#5-General Purpose Elevator, Large, Straight, Curved, 2.2mm Tip, 230mm Length
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- #5-General Purpose Elevator, Large, Straight, Curved, 2.2mm Tip, 230mm Length FDA UDI
- Generic Name
- Periosteal elevator, reusable FDA UDI
- Device Name
- #5-General Purpose Elevator, Large, Straight, Curved, 2.2mm Tip, 230mm Length FDA UDI
- Model / Reference
- N7105E-K FDA UDI
- Description
- #5-General Purpose Elevator, Large, Straight, Curved, 2.2mm Tip, 230mm Length FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840096204568 FDA UDI
- FDA Product Code
- HTE FDA UDI
- GMDN Term
- Periosteal elevator, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
No
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Periosteal elevator, reusable
#5-General Purpose Elevator, Large, Straight, Curved, 2.2mm Tip, 230mm Length by Katalyst Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Periosteal elevator, reusable.
- Ambler Surgical — Ambler Surgical, LLC · Class I
- STERLING — BENCO DENTAL SUPPLY CO. · Class I
- MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
- SCANLAN® Instrumentation — SCANLAN INTERNATIONAL INC · Class I
- BARRIER PLACEMENT INSTRUMENT — W.H. Holden, Inc. · Class I
- ELEVATOR — KLS-Martin L.P. · Class I
- HELMUT ZEPF — Helmut Zepf Medizintechnik GmbH · Class I
- Ambler Surgical — Ambler Surgical, LLC · 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
- Katalyst Surgical, Llc
Sources (1)
- FDA UDI 9de3dd78-3f36-40d9-bb80-02d6ee91b502 33 fields · synced May 30, 2026