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Medis
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref NF207Model NF10; NF20; NF30; NF40; NF11; NF21; NF31; NF41
Identity
- Trade Name
- Nasopharyngeal Airways EUDAMEDMedis FDA UDI
- Generic Name
- Nasopharyngeal airway, single-use FDA UDI
- Device Name
- Nasopharyngeal Airway EUDAMEDwith O2 Port, RespiratoryIndicator, Filter, Soft Tip and 15mm Connector 7.0mm FDA UDI
- Model / Reference
- NF207 EUDAMEDFDA UDINF10; NF20; NF30; NF40; NF11; NF21; NF31; NF41 EUDAMED
- Description
- with O2 Port, RespiratoryIndicator, Filter, Soft Tip and 15mm Connector 7.0mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06920687300238 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
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
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
MR Safe FDA UDI
Category: Nasopharyngeal airway, single-use
Medis by Tianjin Medis Medical Device 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.
- 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
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
- Tianjin Medis Medical Device Co., Ltd.
Sources (2)
- FDA UDI af803d2a-d394-4ee3-8ddc-f2bae4bc7a03 35 fields · synced Jun 19, 2026
- EUDAMED 35e7cb50-59d8-4ae8-8796-82829ec2e589 61 fields · synced Jun 19, 2026