Identity
- Trade Name
- NeoSnug EUDAMEDNeoSnug Small FDA UDI
- Generic Name
- Wearable percutaneous catheter/tube holder FDA UDI
- Device Name
- NeoSnug EUDAMEDNeoSnug is intended to support, secure, and hold gastrointestinal tubes on patients’ skin. 30 per box 5 sets of 2 (Lefth & Right) FDA UDI
- Model / Reference
- N7015-15 EUDAMED20812594012925 FDA UDI
- Description
- NeoSnug is intended to support, secure, and hold gastrointestinal tubes on patients’ skin. 30 per box 5 sets of 2 (Lefth & Right) FDA UDI
Identifiers
- Catalog Number
- N7015-15 FDA UDI
- Primary DI / UDI-DI
- 20812594012925 EUDAMEDFDA UDI
- Basic UDI-DI
- 081259401N70150MB EUDAMED
- FDA Product Code
- PLI FDA UDI
- EMDN Code
- M0599 MEDICAL PLASTERS - OTHER EUDAMED
- GMDN Term
- Wearable percutaneous catheter/tube holder FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.5980 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
NeoSnug 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 | 081259401N70150MB | 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 f4ec610a-7cf7-4a67-8258-be655cd8adab 61 fields · synced Jul 21, 2026
- FDA UDI f281fff2-40a1-4420-be4c-bd5673a65e0b 34 fields · synced May 30, 2026