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ZYNRELEF 10 mL Vial Access Needle (VAN) Replacement
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- ZYNRELEF 10 mL Vial Access Needle (VAN) Replacement FDA UDI
- Generic Name
- Vial/bottle adaptor, non-hermetic FDA UDI
- Device Name
- ZYNRELEF 10 mL Vial Access Needle (VAN) Replacement FDA UDI
- Model / Reference
- N/A FDA UDI
- Description
- ZYNRELEF 10 mL Vial Access Needle (VAN) Replacement FDA UDI
Identifiers
- Catalog Number
- 70016563-00 FDA UDI
- Primary DI / UDI-DI
- 00347426505086 FDA UDI
- FDA Product Code
- LHI FDA UDI
- GMDN Term
- Vial/bottle adaptor, non-hermetic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 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
No
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
Yes
FDA UDI
Category: Vial/bottle adaptor, non-hermetic
ZYNRELEF 10 mL Vial Access Needle (VAN) Replacement by Heron Therapeutics, 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
- Heron Therapeutics, Inc.
Sources (1)
- FDA UDI fc9c93e2-9b45-44bc-8ee9-f38d37e068a3 34 fields · synced May 30, 2026