Identity
- Trade Name
- Dissector FDA UDI
- Generic Name
- Open-surgery dissector FDA UDI
- Device Name
- Articulating Dissection Instrument, 18 cm shaft FDA UDI
- Model / Reference
- GPD1 FDA UDI
- Description
- Articulating Dissection Instrument, 18 cm shaft FDA UDI
Identifiers
- Catalog Number
- A000418 FDA UDI
- Primary DI / UDI-DI
- 00818354010541 FDA UDI
- FDA Product Code
- GDI FDA UDIFTD FDA UDI
- GMDN Term
- Open-surgery dissector FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI878.4580 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
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 18 Centimeter FDA UDI
Category: Open-surgery dissector
Dissector by Atricure, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Open-surgery dissector.
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- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
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
- Atricure, Inc.
Sources (1)
- FDA UDI d7106cc8-d3f2-4c66-8c74-dbd4028174f2 36 fields · synced May 30, 2026