Identity
- Trade Name
- ExtravaStopper FDA UDI
- Generic Name
- Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
- Device Name
- Portal Plug FDA UDI
- Model / Reference
- ESTOP FDA UDI
- Description
- Portal Plug FDA UDI
Identifiers
- Catalog Number
- ESTOP FDA UDI
- Primary DI / UDI-DI
- 00866497000332 FDA UDI
- FDA Product Code
- FGY FDA UDI
- GMDN Term
- Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Radiation Sterilization FDA UDI
Category: Surgical/emergency suction cannula, non-illuminating, single-use
ExtravaStopper by Cannuflow, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical/emergency suction cannula, non-illuminating, single-use.
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- BR Surgical, LLC — BR SURGICAL LLC · Class I
- NETWORK — Network Medical Products, Ltd. · Class I
- Medichoice — OWENS & MINOR DISTRIBUTION, INC. · Class II
- Single Use Professional — EAKIN SURGICAL LIMITED · Class II
- BR Surgical, LLC — BR SURGICAL LLC · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Cannuflow, Inc.
Sources (1)
- FDA UDI 809e7152-09dd-46f3-82ea-940d4d2bf08b 34 fields · synced May 30, 2026