Identity
- Trade Name
- ATEC Needle Guide FDA UDI
- Generic Name
- Needle guide, single-use FDA UDI
- Device Name
- AURORA NEEDLE GUIDE FDA UDI
- Model / Reference
- ATEC NG09-A1 FDA UDI
- Description
- AURORA NEEDLE GUIDE FDA UDI
Identifiers
- Catalog Number
- ATEC NG09-A1 FDA UDI
- Primary DI / UDI-DI
- 05420045503147 FDA UDI
- FDA Product Code
- KNW FDA UDI
- GMDN Term
- Needle guide, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1075 FDA UDI
- 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
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
No
FDA UDI
MR Conditional FDA UDI
ATEC Needle Guide by Hologic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hologic, Inc.
Sources (1)
- FDA UDI 27c1b001-f4ce-4d53-8140-06e3f5cb74a8 36 fields · synced May 30, 2026