Identity
- Trade Name
- SafeSnap 4+ (PolypTrap) FDA UDI
- Generic Name
- Surgical suction system collection container, single-use FDA UDI
- Device Name
- with 4 chambers FDA UDI
- Model / Reference
- SPT-01-04 FDA UDI
- Description
- with 4 chambers FDA UDI
Identifiers
- Catalog Number
- K20000036 FDA UDI
- Primary DI / UDI-DI
- 06936603230008 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- Surgical suction system collection container, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Category: Surgical suction system collection container, single-use
SafeSnap 4+ (PolypTrap) by Yangzhou Fartley Medical Instrument Technology Co., Ltd. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED
Similar devices
Also classified as Surgical suction system collection container, single-use.
- BEMIS — BEMIS MANUFACTURING CO. · Class II
- Bemis — BEMIS MANUFACTURING CO. · Class II
- Berkeley Vacurette — Gyrus Acmi, Inc. · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- Oxygen Tubing Y-Connector — SUNSET HEALTHCARE SOLUTIONS, Inc. · Class II
- SOMAVAC Waste Collection Unit — SOMAVAC MEDICAL SOLUTIONS, INC. · Class I
- Bemis — BEMIS MANUFACTURING CO. · Class II
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 II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
Sources (2)
- FDA UDI 41d5d496-6ec9-427f-a744-1a421fe2b28d 34 fields · synced Jun 19, 2026
- EUDAMED 1 fields · synced Jun 1, 2026