Identity
- Trade Name
- RUSCH FDA UDI
- Generic Name
- Basic endotracheal tube, single-use FDA UDI
- Device Name
- ENDOTRACHEAL TUBE - WITH CUFF - MAGILL - STERILE PACK FDA UDI
- Model / Reference
- IPN041482 FDA UDI
- Description
- ENDOTRACHEAL TUBE - WITH CUFF - MAGILL - STERILE PACK FDA UDI
Identifiers
- Catalog Number
- 112080080 FDA UDI
- Primary DI / UDI-DI
- 14026704341327 FDA UDI
- 510(k) Number
- K961837 FDA UDI
- FDA Product Code
- BTR FDA UDI
- GMDN Term
- Basic endotracheal tube, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5730 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
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 340 Millimeter FDA UDIHeight — 30 Millimeter FDA UDIWidth — 30 Millimeter FDA UDIOuter Diameter — 10.7 Millimeter FDA UDI
Category: Basic endotracheal tube, single-use
Rusch by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Basic endotracheal tube, single-use.
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- Medline Industries, Inc. — MEDLINE INDUSTRIES, INC. · Class II
- Endotracheal Tubes — Dynarex Corp. · Class II
- ULTRAMED ENDOTRACHEAL TUBE ORAL/NASAL CUFFED Size 3 — Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E) · Class IIa
- Rurka intubacyjna z mankietem — SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa · Class IIa
Cleared under the same submission
K961837 also covers:
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
- RUSCH — TELEFLEX INCORPORATED
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
- Teleflex Incorporated
Sources (1)
- FDA UDI 9ad08232-a8e8-473f-a1c2-0c629e1621da 36 fields · synced May 30, 2026