Identity
- Trade Name
- SunMed FDA UDI
- Generic Name
- Nasopharyngeal airway, single-use FDA UDI
- Device Name
- NASO LATEX FREE PVC 3.5MM 14FR FDA UDI
- Model / Reference
- 1-5073-14 FDA UDI
- Description
- NASO LATEX FREE PVC 3.5MM 14FR FDA UDI
Identifiers
- Catalog Number
- 1-5073-14 FDA UDI
- Primary DI / UDI-DI
- 10889483042472 FDA UDI
- FDA Product Code
- BTQ FDA UDI
- GMDN Term
- Nasopharyngeal airway, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5100 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
No
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
Dimensions & Sizes
- Size
- Length — 85 Millimeter FDA UDI
Category: Nasopharyngeal airway, single-use
SunMed by SunMed — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nasopharyngeal airway, single-use.
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- Disposable sterile nasopharyngeal tube — Rmist(Tianjin) Medical Device Co., Ltd. · Class IIa
- Shiley — Covidien LP · Class I
- Disposable sterile nasopharyngeal tube — Rmist(Tianjin) Medical Device Co., Ltd. · 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 I | Pending data |
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Manufacturer
- Manufacturer
- SunMed
Sources (1)
- FDA UDI 89ad50e1-74f1-4ae1-bf5d-3a58147a370d 36 fields · synced May 30, 2026