← Back to catalogue
Airtime Horizontal Drying, Directional Flow Tubing Set
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Airtime Horizontal Drying, Directional Flow Tubing Set FDA UDI
- Generic Name
- Endoscope dryer FDA UDI
- Device Name
- Airtime Horizontal Drying, Directional Flow Tubing Set - 1 Set FDA UDI
- Model / Reference
- HDF200X FDA UDI
- Description
- Airtime Horizontal Drying, Directional Flow Tubing Set - 1 Set FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00843356100518 FDA UDI
- FDA Product Code
- JRJ FDA UDI
- GMDN Term
- Endoscope dryer FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2050 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
No
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: Endoscope dryer
Airtime Horizontal Drying, Directional Flow Tubing Set by Cygnus Medical L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endoscope dryer.
- Dri-Scope Aid - Cabinet - Manifold (M2R) - Series 2310 - Refurbished — TRICOR SYSTEMS · Class I
- Dri-Scope Aid - Port Tubing Kits - Type O/P (10 pack) — TRICOR SYSTEMS · Class I
- Dri-Scope Aid - Jet Stream - Regulator (R1) — TRICOR SYSTEMS · Class I
- Dri-Scope Aid - Cabinet - Manifold (M2) - Series 3308 - Solaire — TRICOR SYSTEMS · Class I
- Dri-Scope Aid - [Gen 2] Cabinet - Manifold (M1) - Series 3308 — TRICOR SYSTEMS · Class I
- Dri-Scope Aid - Cabinet - Pump Ceiling (P3) - Series 1840 - Solaire — TRICOR SYSTEMS · Class I
- Dri-Scope Aid - Connectors Kits -Type O-EBUS (100 pack) — TRICOR SYSTEMS · Class I
- Dri-Scope Aid - Cabinet - Pump Wall (P2) - Series 1840 - Mobile Aspects — TRICOR SYSTEMS · 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
- Cygnus Medical L.l.c.
Sources (1)
- FDA UDI 750883ed-a844-4573-a206-285da27df98c 33 fields · synced Jun 8, 2026