Identity
- Trade Name
- LMA AIRWAY MANAGEMENT FDA UDI
- Generic Name
- Laryngeal mask airway, single-use FDA UDI
- Device Name
- LMA® Flexible PreCurved™ Airway with Pilot Balloon Size 4 FDA UDI
- Model / Reference
- IPN924057 FDA UDI
- Description
- LMA® Flexible PreCurved™ Airway with Pilot Balloon Size 4 FDA UDI
Identifiers
- Catalog Number
- 1B5040 FDA UDI
- Primary DI / UDI-DI
- 15060112319676 FDA UDI
- FDA Product Code
- CAE FDA UDI
- GMDN Term
- Laryngeal mask airway, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5110 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
Yes
FDA UDI
MR Conditional FDA UDI
Category: Laryngeal mask airway, single-use
Lma Airway Management by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Laryngeal mask airway, single-use.
- Laryseal Blue Laryngeal Mask Airway Slimline Pack Size 1.5 — FLEXICARE MEDICAL LIMITED · Class I
- I-GEL PLUS, SUPRAGLOTTIC AIRWAY, SIZE 4, MEDIUM ADULT, 50-90KG — Intersurgical Incorporated · Class I
- Laryseal Clear Laryngeal Mask Airway Size 4 — FLEXICARE MEDICAL LIMITED · Class I
- Laryngeal Mask Airway — HENAN TUOREN MEDICAL DEVICE CO., LTD. · Class IIa
- SourceMark — SOURCEMARK, LLC. · Class I
- Medline — MEDLINE INDUSTRIES, INC. · Class I
- Disposable Laryngeal Mask Airway — Rmist(Tianjin) Medical Device Co., Ltd. · Class IIa
- Disposable Laryngeal Mask Airway — ZHEJIANG HAISHENG MEDICAL DEVICE CO., LTD. · Class IIa
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
- Teleflex Incorporated
Sources (1)
- FDA UDI d3a8369f-c3f5-42c1-99b3-8a27f31a129b 36 fields · synced Jun 8, 2026