Identity
- Trade Name
- Cohen FDA UDI
- Generic Name
- Endobronchial tube FDA UDI
- Device Name
- Cohen Endobronchial Blocker Set FDA UDI
- Model / Reference
- G44122 FDA UDI
- Description
- Cohen Endobronchial Blocker Set FDA UDI
Identifiers
- Catalog Number
- C-AEBTS-9.0-65-SPH-AS FDA UDI
- Primary DI / UDI-DI
- 00827002441224 FDA UDI
- FDA Product Code
- CBI FDA UDI
- GMDN Term
- Endobronchial tube FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5740 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: Endobronchial tube
Cohen by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Endobronchial tube.
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- Endobronchial Tube — Well Lead Medical Co., Ltd · 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
- Cook Incorporated
Sources (1)
- FDA UDI 0f954871-0d5c-418c-b396-037a1d7c351c 36 fields · synced Jun 8, 2026