Identity
- Trade Name
- SITE-SCRUB FDA UDI
- Generic Name
- Intravenous line connector disinfection scrubber FDA UDI
- Device Name
- Site-ScrubTM IPA Device FDA UDI
- Model / Reference
- 3882025 FDA UDI
- Description
- Site-ScrubTM IPA Device FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10801741086936 FDA UDI
- FDA Product Code
- LKB FDA UDI
- GMDN Term
- Intravenous line connector disinfection scrubber FDA UDI
Classification
- Device Class
- U 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Intravenous line connector disinfection scrubber
Site-Scrub by Bard Access Systems, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intravenous line connector disinfection scrubber.
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 U | Pending data |
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Manufacturer
- Manufacturer
- Bard Access Systems, Inc.
Sources (1)
- FDA UDI fb986993-6be3-47eb-a15b-2b0bd4b21073 33 fields · synced Jun 9, 2026