Identity
- Trade Name
- AirLife™ FDA UDI
- Generic Name
- Airway suction catheter FDA UDI
- Device Name
- AirLife™ Meconium Suction Device (Kurtis MSD) FDA UDI
- Model / Reference
- 4530VS FDA UDI
- Description
- AirLife™ Meconium Suction Device (Kurtis MSD) FDA UDI
Identifiers
- Catalog Number
- 4530VS FDA UDI
- Primary DI / UDI-DI
- 10190752144507 FDA UDI
- FDA Product Code
- BTR FDA UDI
- GMDN Term
- Airway suction catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5730 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
Radiation Sterilization FDA UDI
Category: Airway suction catheter
AirLife™ by Airlife, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Airway suction catheter.
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- Closed Suction Catheters — Ningbo Xinwell Medical Technology Co., Ltd. · Class I
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- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Little Sucker Standard TP — Neotech Products LLC · Class II
- Closed Suction Catheters — Ningbo Xinwell Medical Technology Co., Ltd. · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Novo Surgical Inc. — NOVO SURGICAL, 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
- Airlife, Inc.
Sources (1)
- FDA UDI f33ab861-eeeb-4214-b82d-ee7c91defd93 35 fields · synced May 30, 2026