Identity
- Trade Name
- STORZ FDA UDI
- Generic Name
- Microbial medical gas filter, sterile, single-use FDA UDI
- Device Name
- HIGH FLOW INSUFFLATION TUBING WITH FILTER FDA UDI
- Model / Reference
- 20400161S FDA UDI
- Description
- HIGH FLOW INSUFFLATION TUBING WITH FILTER FDA UDI
Identifiers
- Catalog Number
- 20400161S FDA UDI
- Primary DI / UDI-DI
- 00628725004358 FDA UDI
- FDA Product Code
- HIF FDA UDI
- GMDN Term
- Microbial medical gas filter, sterile, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1730 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Microbial medical gas filter, sterile, single-use
Storz by Canadian Hospital Specialties Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Microbial medical gas filter, sterile, single-use.
- VentiShield Adult B/V Filter Flexi Cath Mount D/Swivel Elbow — FLEXICARE MEDICAL LIMITED · Class II
- VentiShield Adult Bacterial Viral Filter — FLEXICARE MEDICAL LIMITED · Class II
- HepaShield Adult Pleated Hydrophobic Bacterial Viral Filter — FLEXICARE MEDICAL LIMITED · Class II
- Pentair — Pentair Filtration Solutions · Class II
- Pentair — Pentair Filtration Solutions · Class II
- VentiShield Adult Bacterial Viral Filter with Luer Port — FLEXICARE MEDICAL LIMITED · Class II
- Pentair — Pentair Filtration Solutions · Class II
- HepaShield Adult Pleated Hydrophobic Bacterial Viral Filter with Luer Port — FLEXICARE MEDICAL LIMITED · 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
- Canadian Hospital Specialties Limited
Sources (1)
- FDA UDI 9a66d9ce-fc88-404d-baf6-05660c7cfa7f 34 fields · synced Jun 8, 2026