Identity
- Trade Name
- EXTEND FDA UDI
- Generic Name
- Tissue extraction bag introducer FDA UDI
- Device Name
- Extend 10mm Specimen Retrieval System, 240mL FDA UDI
- Model / Reference
- NI0240 FDA UDI
- Description
- Extend 10mm Specimen Retrieval System, 240mL FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10850013527509 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Tissue extraction bag introducer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Tissue extraction bag introducer
Extend by Dannik LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tissue extraction bag introducer.
- SUPERBAG — Dannik LLC · Class II
- SUPERBAG — Dannik LLC · Class II
- SUPERBAG — Dannik LLC · Class II
- EXTEND — Dannik LLC · Class II
- SUPERBAG — Dannik LLC · Class II
- EXTEND — Dannik LLC · Class II
- SOLOBAG — Dannik LLC · Class II
- SUPERBAG — Dannik LLC · 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Dannik LLC
Sources (1)
- FDA UDI 766a8801-1dc7-4449-8ceb-b29117d6327e 33 fields · synced Jun 1, 2026