Identity
- Trade Name
- neoprobe FDA UDI
- Generic Name
- Single-hole nuclear medicine system collimator, straight-bore FDA UDI
- Device Name
- 14 mm Collimator, Model 1013 FDA UDI
- Model / Reference
- NPE14 FDA UDI
- Description
- 14 mm Collimator, Model 1013 FDA UDI
Identifiers
- Catalog Number
- NPE14 FDA UDI
- Primary DI / UDI-DI
- 00841911100324 FDA UDI
- FDA Product Code
- IZD FDA UDI
- GMDN Term
- Single-hole nuclear medicine system collimator, straight-bore FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1320 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Single-hole nuclear medicine system collimator, straight-bore
neoprobe by Devicor Medical Products, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Devicor Medical Products, Inc.
Sources (1)
- FDA UDI 74cacb01-4f98-47df-9f77-162126fc0709 36 fields · synced Jun 8, 2026