Nasopharyngeal Airway
EUDAMEDFDA UDIClass I (EU MDR)
Identity
- Trade Name
- Nasopharyngeal Airway EUDAMEDMedis FDA UDI
- Generic Name
- Nasopharyngeal airway, single-use FDA UDI
- Device Name
- Nasopharyngeal Airway EUDAMEDwith O2 Port,Soft Tip and 15mm Connector 6.0mm FDA UDI
- Model / Reference
- NF10; NF20; NF30; NF40; NF11; NF21; NF31; NF41 EUDAMEDNF106 EUDAMEDFDA UDI
- Description
- with O2 Port,Soft Tip and 15mm Connector 6.0mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06920687300160 EUDAMEDFDA UDI
- Basic UDI-DI
- 69206873NF001KR EUDAMED
- FDA Product Code
- BTQ FDA UDI
- EMDN Code
- R010101 NASOPHARYNGEAL TUBES EUDAMED
- GMDN Term
- Nasopharyngeal airway, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 868.5100 FDA UDI
- Market of Registration
- Spain EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
Yes
Category: Nasopharyngeal airway, single-use
Nasopharyngeal Airway by Tianjin Medis Medical Device Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nasopharyngeal airway, single-use.
- Naso-Pharyngeal Airway — HANGZHOU FORMED MEDICAL DEVICES CO., LTD. · Class I
- RUSCH — TELEFLEX INCORPORATED · Class I
- BM Nasopharyngeal Airways — Bonree Medical Co., Ltd. · Class I
- Shiley — Covidien LP · Class I
- 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
- Adjustable Reconstruction Tube — HOOD, E BENSON LABORATORIES INC · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 69206873NF001KR | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Tianjin Medis Medical Device Co., Ltd.
- EUDAMED SRN
- CN-MF-000020126
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (2)
- EUDAMED 77b1cda5-f857-45bc-8212-4215484911a2 61 fields · synced Oct 6, 2026
- FDA UDI ee4b36df-9a58-4d81-9f2c-9f8d627602eb 35 fields · synced May 29, 2026