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Suction Caddy™ Suction Device Holder
EUDAMEDFDA UDIClass I (EU MDR)
Ref N245Model Suction Caddy™
Identity
- Trade Name
- Suction Caddy™ Suction Device Holder EUDAMEDSuction Caddy™ FDA UDI
- Generic Name
- Airway suction catheter FDA UDI
- Device Name
- Suction Caddy™ EUDAMEDThe Suction Caddy is intended to hold and store a suction device. FDA UDI
- Model / Reference
- Suction Caddy™ EUDAMEDN245 EUDAMEDStandard FDA UDI
- Description
- The Suction Caddy is intended to hold and store a suction device. FDA UDI
Identifiers
- Catalog Number
- N245 FDA UDI
- Primary DI / UDI-DI
- 10812594010313 EUDAMEDFDA UDI
- Basic UDI-DI
- 081259401N24500LM EUDAMED
- FDA Product Code
- JOL FDA UDI
- EMDN Code
- V028099 NEONATOLOGY AND PEDIATRICS DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
- GMDN Term
- Airway suction catheter FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Suction Caddy™ Suction Device Holder by Neotech Products LLC — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 081259401N24500LM | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Neotech Products LLC
- EUDAMED SRN
- US-MF-000001895
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED 8053d284-361d-402a-b208-fd68bf65a8a8 61 fields · synced Jul 12, 2026
- FDA UDI 81b72437-7dce-4904-8a1c-d133dec92794 34 fields · synced May 30, 2026