Identity
- Trade Name
- NAMIC FDA UDI
- Generic Name
- Invasive blood pressure monitoring tubing set FDA UDI
- Device Name
- PRESSURE MONITORING LINE 24" FDA UDI
- Model / Reference
- 90701242 FDA UDI
- Description
- PRESSURE MONITORING LINE 24" FDA UDI
Identifiers
- Primary DI / UDI-DI
- H965907012420 FDA UDI
- FDA Product Code
- DRI FDA UDI
- GMDN Term
- Invasive blood pressure monitoring tubing set FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.2620 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
- Length — 24 Inch FDA UDI
Category: Invasive blood pressure monitoring tubing set
Namic by Navilyst Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Invasive blood pressure monitoring tubing set.
- GE Compatible Adult NIBP Hose, 8 ft, Dual, Female Threaded BP09 Connectors — CABLES AND SENSORS, LLC · Class II
- EASY VENT(TM) EDE-001 — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- CRITIFLO(TM) TA4004 (3ML/HR) — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- COMP PRLINE MF 80 IN (200CM) CLR — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- NAMIC — MEDLINE INDUSTRIES, INC. · Class I
- Connecting Tube — Tianck Medical Co., Ltd. · Class II
- GE Dinamap NIBP Hose: Adult NIBP Hose — CABLES AND SENSORS, LLC · Class II
- COMP PRLINE MM 100CM CLR — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Navilyst Medical, Inc.
Sources (1)
- FDA UDI 57d7a44b-f1e9-4572-b07e-22c1f12c6f5a 35 fields · synced Jun 8, 2026