# Purebrand Slutions Ltd (foreign exporter, London England, GB): 49 new FDA device listings, incl. tubing, noninvasive

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Purebrand Slutions Ltd |
| Owner / operator | Purebrand Solutions LTD |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | London England, GB |
| New listings | 49 |
| Devices | Tubing, Noninvasive; Gastrointestinal Tubes With Enteral Specific Connectors; Tubes, Gastrointestinal (And Accessories); Dressing, Wound, Drug; Container, Specimen, Sterile; Insufflator, Laparoscopic; Laparoscope, General & Plastic Surgery; Apparatus, Exhaust, Surgical; Electrosurgical, Cutting & Coagulation & Accessories; Cannula, Ophthalmic |
| Product codes | GAZ, PIF, KNT, FRO, FMH, HIF, GCJ, FYD, GEI, HMX, MND, HQP, DQX, MDM, HNY |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | General Hospital, Gastroenterology, Urology, Pathology, Obstetrics/Gynecology, General, Plastic Surgery, Ophthalmic, Cardiovascular, Clinical Chemistry |
| Brand names | CARDINAL MEDI-VAC TUBING,SUCTION,NONINVASIVE; COOK-TUBES, GASTROINTESTINAL INTRODUCER SHEATH (AND ACCESSORIES); MOLNLYCKE MEPILEX AG ANTIMICROBIAL FOAM DRESSING WITH SILVER; Conmed Core tubing, noninvasive; BD TUBE, CONTAINER, VACUTAINER; Conmed Tri-Lumen Insufflator, laparoscopic; Conmed Buffalo filter,Adapter, exhaust, surgical; Beaver Visitec Cannula, Ophthalmic |
| First new listing | 2026-06-03 |
| Latest new listing | 2026-09-17 |
| FDA registration number | 3041276591 |
| Registration expires | 2026-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

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.