Identity
- Trade Name
- INTERMITTENT INJECTION SITE FDA UDI
- Generic Name
- Intravenous administration tubing extension set FDA UDI
- Device Name
- "The product is a simple injection/aspiration port which will be sold by itself. It terminates in a male luer taper which can be mated with any femail luer tapered lumen in a device, such as a catheter, communicating with blood or other body fluids. The port occludes the lumen of the catheter or other device. It also provides a latex septum for injection of fluids, including medication, or for aspiration of blood or fluids for testing, ETC. The septum is no-slitted. The Product is discarded when the main device is changed. This product comes with a luer protector cap which is removed and discarded before attaching the port to the catheter or device. This product is not specifically designed for use in hemodialysis systems." FDA UDI
- Model / Reference
- INT-01 FDA UDI
- Description
- "The product is a simple injection/aspiration port which will be sold by itself. It terminates in a male luer taper which can be mated with any femail luer tapered lumen in a device, such as a catheter, communicating with blood or other body fluids. The port occludes the lumen of the catheter or other device. It also provides a latex septum for injection of fluids, including medication, or for aspiration of blood or fluids for testing, ETC. The septum is no-slitted. The Product is discarded when the main device is changed. This product comes with a luer protector cap which is removed and discarded before attaching the port to the catheter or device. This product is not specifically designed for use in hemodialysis systems." FDA UDI
Identifiers
- Catalog Number
- INT-01 FDA UDI
- Primary DI / UDI-DI
- 00646311500015 FDA UDI
- FDA Product Code
- FOZ FDA UDI
- GMDN Term
- Intravenous administration tubing extension set FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5200 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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Intravenous administration tubing extension set
Intermittent Injection Site by Sb-Kawasumi Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Sb-Kawasumi Laboratories, Inc.
Sources (1)
- FDA UDI f4395270-414d-4a04-a0fd-58186115a31b 35 fields · synced Jun 8, 2026