Identity
- Trade Name
- Standard Tube Forceps 18cm FDA UDI
- Generic Name
- Airway tube forceps, reusable FDA UDI
- Device Name
- A hand-held instrument used for grasping a tube [e.g., a catheter or an endotracheal (ET) tube] for its insertion and/or extraction into/from the airways, or for grasping obstructive objects for their removal from the airways. Commonly known as a Magill's forceps, it typically has a scissors-like design with ring handles and is made of high-grade stainless steel. It is available in various sizes and the working end will typically have grasping blades that have small ringed loops or S-shaped distal working ends. The blades are serrated to provide extra grip. It is typically used by emergency medical services (EMS). This is a reusable device. FDA UDI
- Model / Reference
- 03-051-18 FDA UDI
- Description
- A hand-held instrument used for grasping a tube [e.g., a catheter or an endotracheal (ET) tube] for its insertion and/or extraction into/from the airways, or for grasping obstructive objects for their removal from the airways. Commonly known as a Magill's forceps, it typically has a scissors-like design with ring handles and is made of high-grade stainless steel. It is available in various sizes and the working end will typically have grasping blades that have small ringed loops or S-shaped distal working ends. The blades are serrated to provide extra grip. It is typically used by emergency medical services (EMS). This is a reusable device. FDA UDI
Identifiers
- Catalog Number
- 03-051-18 FDA UDI
- Primary DI / UDI-DI
- G25003051180 FDA UDI
- FDA Product Code
- HTD FDA UDI
- GMDN Term
- Airway tube forceps, 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
Dimensions & Sizes
- Size
- Length — 18 Centimeter FDA UDI
Category: Airway tube forceps, reusable
Standard Tube Forceps 18cm by N S Surgical Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Airway tube forceps, reusable.
- Ambler Surgical — Ambler Surgical, LLC · Class I
- Professional Surgical Instruments Co., Inc. — Professional Surgical Instruments Co., Inc. · Class I
- FENTEX — FENTEX medical GmbH · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- BOSS Instruments — Boss Instruments, Ltd. · Class I
- Sklar® — Sklar Corporation · Class I
- Sklar — Sklar Corporation · Class I
- Grafco — GF Health Products, 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 |
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Manufacturer
- Manufacturer
- N S Surgical Company
Sources (1)
- FDA UDI 334d831f-76f0-4f19-89ba-bbb4490e36b0 35 fields · synced Jun 1, 2026