Identity
- Trade Name
- Pusher/Extender FDA UDI
- Generic Name
- Spinal endoscopic-access system FDA UDI
- Model / Reference
- 11-2335 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00846338001834 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Spinal endoscopic-access system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Category: Spinal endoscopic-access system
Pusher/Extender by Elliquence Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- ENDOSPINE — Karl Storz GmbH & Co. KG · Class II
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 |
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Manufacturer
- Manufacturer
- Elliquence Llc
Sources (1)
- FDA UDI 78d83159-f7cf-44fd-8b27-3e414cc6a9f3 32 fields · synced Jun 6, 2026