Identity
- Trade Name
- Temena FDA UDI
- Generic Name
- Peripheral nerve-block sharp needle FDA UDI
- Device Name
- Needle for peripheral nerve blocks 24G x 25 mm FDA UDI
- Model / Reference
- 02025-24 FDA UDI
- Description
- Needle for peripheral nerve blocks 24G x 25 mm FDA UDI
Identifiers
- Catalog Number
- 02025-24 FDA UDI
- Primary DI / UDI-DI
- 03700339710201 FDA UDI
- FDA Product Code
- GXZ FDA UDI
- GMDN Term
- Peripheral nerve-block sharp needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1350 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 25 Millimeter FDA UDINeedle Gauge — 24 Gauge FDA UDI
Category: Peripheral nerve-block sharp needle
Temena by Te ME NA Sas — 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
- Te ME NA Sas
Sources (1)
- FDA UDI 4719f241-c0ff-48e6-a0cd-f02988b4b31a 35 fields · synced May 29, 2026