Identity
- Trade Name
- Interlink FDA UDI
- Generic Name
- Luer/Luer linear connector, single-use FDA UDI
- Device Name
- Syringe Cannula FDA UDI
- Model / Reference
- 303366 FDA UDI
- Description
- Syringe Cannula FDA UDI
Identifiers
- Catalog Number
- 303366 FDA UDI
- Primary DI / UDI-DI
- 00382903033669 FDA UDI
- 510(k) Number
- K920422 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- Luer/Luer linear connector, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 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
No
FDA UDI
Category: Luer/Luer linear connector, single-use
Interlink by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K920422 also covers:
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
- Becton Dickinson And Company
Sources (1)
- FDA UDI ad523539-c1ff-44e2-ac01-6095cf74eb0f 36 fields · synced Jun 8, 2026