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NeoGrip® Tubing and Cable Holder - Blue
EUDAMEDFDA UDIClass I (EU MDR)
Ref N602BModel NeoGrip®
Identity
- Trade Name
- NeoGrip® Tubing and Cable Holder - Blue EUDAMEDNeoGrip® FDA UDI
- Generic Name
- Wearable percutaneous catheter/tube holder FDA UDI
- Device Name
- NeoGrip® EUDAMEDThe NeoGrip/VersaGrip is intended to organize tubes, cables and circuits. FDA UDI
- Model / Reference
- NeoGrip® EUDAMEDN602B EUDAMEDBlue FDA UDI
- Description
- The NeoGrip/VersaGrip is intended to organize tubes, cables and circuits. FDA UDI
Identifiers
- Catalog Number
- N602B FDA UDI
- Primary DI / UDI-DI
- 10812594010726 EUDAMEDFDA UDI
- Basic UDI-DI
- 081259401N60100LH EUDAMED
- FDA Product Code
- JAY FDA UDI
- EMDN Code
- R028002 RESPIRATORY CIRCUITS SUPPORTS EUDAMED
- GMDN Term
- Wearable percutaneous catheter/tube holder FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 868.5280 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
No
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
NeoGrip® Tubing and Cable Holder - Blue 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 | 081259401N60100LH | 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 b68f6cda-d4bd-4ab4-9a18-07ecfc0a96b2 61 fields · synced Jun 17, 2026
- FDA UDI 98a799ef-1e5f-496f-b398-cb2c012d00ce 34 fields · synced May 30, 2026