Identity
- Trade Name
- Integra® FDA UDI
- Generic Name
- Peripheral nerve-block blunt needle access cannula FDA UDI
- Device Name
- NERVE BLOCK TRAY FDA UDI
- Model / Reference
- 3404962 FDA UDI
- Description
- NERVE BLOCK TRAY FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10381780265405 FDA UDI
- GMDN Term
- Peripheral nerve-block blunt needle access cannula FDA UDI
Classification
- Commercial Distribution
- Not 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
Yes
FDA UDI
Combination Product
Yes
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
Integra nerve block tray is a sterile, single-use device designed to provide percutaneous access to a peripheral nerve group for the insertion of a nerve-block blunt needle and injection of an anaesthetic/analgesic agent for pain control. This flexible tube is typically made of plastic with a sharp-tipped metal needle for easy introduction and removal.
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Integra Pain Management
Sources (1)
- FDA UDI 992ea642-e67f-4077-8645-baa6ad4153b1 36 fields · synced Jun 20, 2026