Identity
- Trade Name
- Parker Flex-Tip FDA UDI
- Generic Name
- Endobronchial tube FDA UDI
- Device Name
- Parker Endo-Bronch with Standard Tip (Right Double-lumen Endobronchial Tube), PSTDR, 41 Fr, O.D 12.0mm, I.D 5.0mm FDA UDI
- Model / Reference
- H-PSTDR-41 FDA UDI
- Description
- Parker Endo-Bronch with Standard Tip (Right Double-lumen Endobronchial Tube), PSTDR, 41 Fr, O.D 12.0mm, I.D 5.0mm FDA UDI
Identifiers
- Catalog Number
- H-PSTDR-41 FDA UDI
- Primary DI / UDI-DI
- 10749065861504 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
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 12 Millimeter FDA UDI
Category: Endobronchial tube
Parker Flex-Tip by Salter Labs — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endobronchial tube.
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- SILBRONCHO (RIGHT LUNG) — Fuji Systems Corp. · 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
- Salter Labs
Sources (1)
- FDA UDI a42d0892-3124-4e40-acb1-700ab002c0ba 37 fields · synced Jun 8, 2026