# Cbr Enterprise Limited (foreign exporter, Hong Kong, HK): 59 new FDA device listings, incl. tubes, vials, systems, serum separators, blood collection

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Cbr Enterprise Limited |
| Owner / operator | CBR Enterprise Limited |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | Hong Kong, HK |
| New listings | 59 |
| Devices | Tubes, Vials, Systems, Serum Separators, Blood Collection; Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System; Humidifier, Respiratory Gas, (Direct Patient Interface); Drain, Tee (Water Trap); Set, Tubing, Blood, With And Without Anti-Regurgitation Valve; Filter, Infusion Line; Set, Administration, Intravascular; Floss, Dental; Laparoscope, General & Plastic Surgery; Insufflator, Laparoscopic |
| Product codes | JKA, ONB, BTT, BYH, FJK, FPB, FPA, JES, GCJ, HIF, FFF, CCL, NHP, NHQ, BZK |
| Device classes | Class I, Class II, Class III |
| Medical specialties | Clinical Chemistry, General Hospital, Anesthesiology, Gastroenterology, Urology, Dental, Obstetrics/Gynecology, General, Plastic Surgery, Cardiovascular, Orthopedic, Clinical Toxicology, Physical Medicine |
| Brand names | CONNECTOR; Set, administration, intravascular; COVER,PROBE,CLEAN,TROPHON; SPIROMETER, MONITORING; SLEEVE, LIMB, COMPRESSIBLE; PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR |
| First new listing | 2026-05-14 |
| Latest new listing | 2026-10-23 |
| FDA registration number | 3013557562 |
| Registration expires | 2027-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- Listed in the last 45 days.

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.