Identity
- Trade Name
- ELMED INCORPORATED FDA UDI
- Generic Name
- Vascular dilator, reusable FDA UDI
- Device Name
- 2 PIECE SHUNT PERITONEAL CATHETER PASSER W/ T HANDLE AND FEMALE LUER LOCK, CANNULA: 4.2 DIA. O.D., 3.6MM DIA. I.D.-38CM WORKING LENGTH, PROBE: 3.5MM DIA. AT TIP, 44CM WORKING LENGTH REUSABLE STAINLESS STEEL, 46CM OVERALL LENGTH FDA UDI
- Model / Reference
- 23-1715 FDA UDI
- Description
- 2 PIECE SHUNT PERITONEAL CATHETER PASSER W/ T HANDLE AND FEMALE LUER LOCK, CANNULA: 4.2 DIA. O.D., 3.6MM DIA. I.D.-38CM WORKING LENGTH, PROBE: 3.5MM DIA. AT TIP, 44CM WORKING LENGTH REUSABLE STAINLESS STEEL, 46CM OVERALL LENGTH FDA UDI
Identifiers
- Catalog Number
- 23-1715 FDA UDI
- Primary DI / UDI-DI
- 00198506082511 FDA UDI
- FDA Product Code
- PIY FDA UDI
- GMDN Term
- Vascular dilator, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4545 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Vascular dilator, reusable
Elmed Incorporated by Elmed Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Marina Medical — MARINA MEDICAL INSTRUMENTS, 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 |
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Manufacturer
- Manufacturer
- Elmed Incorporated
Sources (1)
- FDA UDI f146c443-159f-4c5f-8da2-286602485025 35 fields · synced Jun 8, 2026