← Back to catalogue
GP General Purpose Drainage Catheter
FDA UDIClass I (US FDA UDI)
by Uresil Corp.
Identity
- Trade Name
- GP General Purpose Drainage Catheter FDA UDI
- Generic Name
- Suction system catheter, general-purpose FDA UDI
- Device Name
- HYDROPHILIC COATED MINI-PIGTAIL LOCKING CATHETER WITH DEPTH MARKS, 8F FDA UDI
- Model / Reference
- MPL2T-0830H FDA UDI
- Description
- HYDROPHILIC COATED MINI-PIGTAIL LOCKING CATHETER WITH DEPTH MARKS, 8F FDA UDI
Identifiers
- Catalog Number
- MPL2T-0830H FDA UDI
- Primary DI / UDI-DI
- 00817640021001 FDA UDI
- FDA Product Code
- GBO FDA UDI
- GMDN Term
- Suction system catheter, general-purpose FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 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
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
- Catheter Gauge — 8 French FDA UDILength — 25 Centimeter FDA UDI
Category: Suction system catheter, general-purpose
GP General Purpose Drainage Catheter by Uresil Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Suction system catheter, general-purpose.
- Integra® Ruggles®-Redmond™ — Integra LifeSciences Production Corporation · Class II
- Gen2 — SURGIX MEDICAL LLC · Class II
- Hayden Medical — Hayden Medical Inc · Class II
- Gen2 — SURGIX MEDICAL LLC · Class II
- Integra® Jarit® — Integra LifeSciences Production Corporation · Class II
- Gen2 — SURGIX MEDICAL LLC · Class II
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Uresil Corp.
Sources (1)
- FDA UDI b0ce245e-dd25-4f84-8ded-0edcc872688a 36 fields · synced May 30, 2026