Identity
- Trade Name
- Nasopharyngeal airway FDA UDI
- Generic Name
- Nasopharyngeal airway, single-use FDA UDI
- Device Name
- Nasopharyngeal airway Slidable type14Fr FDA UDI
- Model / Reference
- A06A043510 FDA UDI
- Description
- Nasopharyngeal airway Slidable type14Fr FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06944932752122 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
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: Nasopharyngeal airway, single-use
Nasopharyngeal airway by Well Lead Medical Co., Ltd — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Nasopharyngeal airway, single-use.
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- Shiley — Covidien LP · Class I
- Disposable sterile nasopharyngeal tube — Rmist(Tianjin) Medical Device Co., Ltd. · Class IIa
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Well Lead Medical Co., Ltd
Sources (2)
- FDA UDI 4895cbbb-7ee6-4c9d-b27a-c75b88136e04 33 fields · synced Oct 6, 2026
- EUDAMED 1 fields · synced Jun 18, 2026