Identity
- Trade Name
- Curaplex FDA UDI
- Generic Name
- Intravenous line recessed-needle connector FDA UDI
- Device Name
- Curaplex CuraSlide BC Safety IV Catheter w/ Blood Control, 22ga x 1in L, Blue FDA UDI
- Model / Reference
- 1613-86222 FDA UDI
- Description
- Curaplex CuraSlide BC Safety IV Catheter w/ Blood Control, 22ga x 1in L, Blue FDA UDI
Identifiers
- Catalog Number
- 1613-86222 FDA UDI
- Primary DI / UDI-DI
- 00810094574192 FDA UDI
- FDA Product Code
- FOZ FDA UDI
- GMDN Term
- Intravenous line recessed-needle connector 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 line recessed-needle connector
Curaplex by Bound Tree Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Intravenous line recessed-needle connector.
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- Smith's Catheters — MEDSOURCE INTERNATIONAL LLC · Class II
- Smith's Catheters — MEDSOURCE INTERNATIONAL LLC · Class II
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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
- Bound Tree Medical, Llc
Sources (1)
- FDA UDI d3b106ec-db4b-4663-9ca5-5241f8f831f6 34 fields · synced May 30, 2026