Identity
- Trade Name
- PILLING FDA UDI
- Generic Name
- Suction system catheter, general-purpose FDA UDI
- Device Name
- SUCTION TIP FOR 351500 FDA UDI
- Model / Reference
- IPN005364 FDA UDI
- Description
- SUCTION TIP FOR 351500 FDA UDI
Identifiers
- Catalog Number
- 351501 FDA UDI
- Primary DI / UDI-DI
- 24026704517194 FDA UDI
- FDA Product Code
- BYY FDA UDI
- GMDN Term
- Suction system catheter, general-purpose FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Length — 0.375 Inch FDA UDI
Category: Suction system catheter, general-purpose
Pilling by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Suction system catheter, general-purpose.
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- Gen2 — SURGIX MEDICAL LLC · Class II
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- Gen2 — SURGIX MEDICAL LLC · Class II
- GP General Purpose Drainage Catheter — Uresil Corp. · Class I
- Integra® Jarit® — Integra LifeSciences Production Corporation · Class II
- Gen2 — SURGIX MEDICAL LLC · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI b5cf085c-da6e-495e-a714-3b019ace7a4b 36 fields · synced Jun 1, 2026