Identity
- Trade Name
- Argyle FDA UDI
- Generic Name
- Pleuroscopic/mediastinoscopic trocar blade FDA UDI
- Device Name
- Trocar Catheter,Sharp Tip FDA UDI
- Model / Reference
- 8888561076 FDA UDI
- Description
- Trocar Catheter,Sharp Tip FDA UDI
Identifiers
- Catalog Number
- 8888561076 FDA UDI
- Primary DI / UDI-DI
- 10884521029316 FDA UDI
- FDA Product Code
- DRC FDA UDI
- GMDN Term
- Pleuroscopic/mediastinoscopic trocar blade FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1390 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
Yes
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
Dimensions & Sizes
- Size
- Length — 15.75 Inch FDA UDICatheter Gauge — 32 French FDA UDI
Category: Pleuroscopic/mediastinoscopic trocar blade
Argyle by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pleuroscopic/mediastinoscopic trocar blade.
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- Wexler Surgical, Inc. — Wexler Surgical, Inc. · Class II
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- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
- Wexler Surgical, Inc. — Wexler Surgical, Inc. · Class II
- Wexler Surgical, Inc. — Wexler Surgical, Inc. · Class II
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
- Argyle — Cardinalhealth · Class II
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
- Cardinalhealth
Sources (1)
- FDA UDI f6d9ec9d-5a33-404c-bb90-2976b6c63787 37 fields · synced May 30, 2026