Identity
- Trade Name
- LMA FDA UDI
- Generic Name
- Basic endotracheal tube, single-use FDA UDI
- Device Name
- LMA Fastrach Combo-Kit, SU, Size 3 FDA UDI
- Model / Reference
- IPN042410 FDA UDI
- Description
- LMA Fastrach Combo-Kit, SU, Size 3 FDA UDI
Identifiers
- Catalog Number
- 135230 FDA UDI
- Primary DI / UDI-DI
- 05060112311888 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
Yes
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
MR Conditional FDA UDI
Category: Basic endotracheal tube, single-use
Lma by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Basic endotracheal tube, single-use.
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- 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
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 33e31b83-06a5-4f0f-bfc4-afe1c85b3754 36 fields · synced May 30, 2026