Identity
- Trade Name
- QUICK-FIT, PINK TOP CANISTER 3000cc FDA UDI
- Generic Name
- Surgical suction system collection container, reusable FDA UDI
- Device Name
- Canister, Quick-Fit, Pink Top Canister 3000cc, Reusable, for use with Quick-Fit, Pink Top Liners 3000cc (P/N: 20-5155-00) FDA UDI
- Model / Reference
- 20515600 FDA UDI
- Description
- Canister, Quick-Fit, Pink Top Canister 3000cc, Reusable, for use with Quick-Fit, Pink Top Liners 3000cc (P/N: 20-5155-00) FDA UDI
Identifiers
- Catalog Number
- 20-5156-00 FDA UDI
- Primary DI / UDI-DI
- B458205156000 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- Surgical suction system collection container, reusable 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
No
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, reusable
QUICK-FIT, PINK TOP CANISTER 3000cc by The Wells Johnson Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical suction system collection container, reusable.
- DeRoyal — PERGO MEDIKAL VE ILAC SANAYI ANONIM SIRKETI · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- Allied Medical LLC — Allied Medical LLC · Class II
- LOWER SEAL FOR MICTEC GLASS BOTTLE — SONTEC INSTRUMENTS, INC. · Class II
- Large lid with conical patient connection 6–10 mm — Medela LLC · Class II
- Lid for safety Set with overflow protection device — Medela LLC · Class II
- Suction jar polysulfone 3l — Medela LLC · Class II
- Allied Medical LLC — Allied Medical LLC · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| 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
- Manufacturer
- The Wells Johnson Company
Sources (1)
- FDA UDI 00389034-900f-4dee-9251-b45132dc0ec5 34 fields · synced Jun 1, 2026