Identity
- Trade Name
- Curaplex FDA UDI
- Generic Name
- General-purpose syringe, single-use FDA UDI
- Device Name
- *Custom* St. Paul Fire IGEL Airway Kit Size LARGE FDA UDI
- Model / Reference
- 8600-01212 FDA UDI
- Description
- *Custom* St. Paul Fire IGEL Airway Kit Size LARGE FDA UDI
Identifiers
- Catalog Number
- 8600-01212 FDA UDI
- Primary DI / UDI-DI
- 00817617021324 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- General-purpose syringe, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose syringe, single-useLaryngeal mask airway, single-use
Curaplex by Bound Tree Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- I-GEL PLUS, SUPRAGLOTTIC AIRWAY, SIZE 4, MEDIUM ADULT, 50-90KG — Intersurgical Incorporated · Class I
- LMA AIRWAY MANAGEMENT — TELEFLEX INCORPORATED · Class I
- LMA AIRWAY MANAGEMENT — TELEFLEX INCORPORATED · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bound Tree Medical, Llc
Sources (1)
- FDA UDI ee4b0dce-367a-44a8-9106-2463a72b2f54 34 fields · synced Jun 1, 2026