# Ningbo Greetmed Medical Instruments Co., Ltd. (specification developer, Ningbo Zhejiang, CN): 2 new FDA device listings, incl. electrode, electrocardiograph

**Score:** 60/100

| Field | Value |
|---|---|
| Establishment | Ningbo Greetmed Medical Instruments Co., Ltd. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Ningbo Zhejiang, CN |
| New listings | 2 |
| Devices | Electrode, Electrocardiograph; Airway, Oropharyngeal, Anesthesiology |
| Product codes | DRX, CAE |
| Device classes | Class I, Class II |
| Medical specialties | Cardiovascular, Anesthesiology |
| Brand names | ECG electrode; Oropharyngeal Airways; guedel airway |
| First new listing | 2026-08-19 |
| Latest new listing | 2026-09-14 |
| FDA registration number | 3008496560 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.