← Back to catalogue
SOLUS FLEXIBLE WIRE REINFORCED LARYNGEAL MASK AIRWAY SIZE 4 MEDIUM ADULT 50-70kg
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- SOLUS FLEXIBLE WIRE REINFORCED LARYNGEAL MASK AIRWAY SIZE 4 MEDIUM ADULT 50-70kg FDA UDI
- Generic Name
- Laryngeal mask airway, single-use FDA UDI
- Device Name
- SOLUS FLEXIBLE, WIRE REINFORCED LARYNGEAL MASK AIRWAY, SIZE 4, MEDIUM ADULT, 50-70KG FDA UDI
- Model / Reference
- 8004001 FDA UDI
- Description
- SOLUS FLEXIBLE, WIRE REINFORCED LARYNGEAL MASK AIRWAY, SIZE 4, MEDIUM ADULT, 50-70KG FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05030267073559 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
Yes
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
Category: Laryngeal mask airway, single-use
SOLUS FLEXIBLE WIRE REINFORCED LARYNGEAL MASK AIRWAY SIZE 4 MEDIUM ADULT 50-70kg by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Laryngeal mask airway, single-use.
- LMA AIRWAY MANAGEMENT — TELEFLEX INCORPORATED · Class I
- LMA AIRWAY MANAGEMENT — TELEFLEX INCORPORATED · Class I
- Laryseal Blue Laryngeal Mask Airway Slimline Pack Size 1.5 — FLEXICARE MEDICAL LIMITED · Class I
- LMA AIRWAY MANAGEMENT — TELEFLEX INCORPORATED · Class I
- LMA — TELEFLEX INCORPORATED · Class I
- LMA AIRWAY MANAGEMENT — TELEFLEX INCORPORATED · Class I
- LMA AIRWAY MANAGEMENT — TELEFLEX INCORPORATED · Class I
- Laryseal Clear Laryngeal Mask Airway Size 4 — FLEXICARE MEDICAL LIMITED · 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
- Intersurgical Incorporated
Sources (1)
- FDA UDI cf25a48f-9660-4764-8671-c1d52976db12 34 fields · synced Jun 8, 2026