Identity
- Trade Name
- Arndt FDA UDI
- Generic Name
- Endotracheal tube guide, single-use FDA UDI
- Device Name
- Arndt Airway Exchange Catheter FDA UDI
- Model / Reference
- G11920 FDA UDI
- Description
- Arndt Airway Exchange Catheter FDA UDI
Identifiers
- Catalog Number
- C-CAE-14.0-70-LMA FDA UDI
- Primary DI / UDI-DI
- 00827002119208 FDA UDI
- FDA Product Code
- LRC FDA UDI
- GMDN Term
- Endotracheal tube guide, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Endotracheal tube guide, single-use
Arndt by Cook Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Endotracheal tube guide, single-use.
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- JEM 355 Endotracheal Tube Changer — INSTRUMENTATION INDUSTRIES, INCORPORATED · Class II
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
- Cook Incorporated
Sources (1)
- FDA UDI 580dc6e3-8faa-496d-a8ec-18306ef63fa7 36 fields · synced Jun 8, 2026