Identity
- Trade Name
- Bone Access Needle FDA UDI
- Generic Name
- Bone access cannula FDA UDI
- Device Name
- Bone Access Needle 11ga x 4in FDA UDI
- Model / Reference
- DBANM1104TL FDA UDI
- Description
- Bone Access Needle 11ga x 4in FDA UDI
Identifiers
- Catalog Number
- DBANM1104TL FDA UDI
- Primary DI / UDI-DI
- 00886333222957 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Bone access cannula FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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: Bone access cannula
Bone Access Needle by Argon Medical Devices, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Argon Medical Devices, Inc.
Sources (1)
- FDA UDI 432c0cc9-0d75-4778-a176-8c04d7dff6a1 37 fields · synced Jun 9, 2026