Identity
- Trade Name
- Retractor EUDAMEDLife Instruments FDA UDI
- Generic Name
- Surgical retractor/retraction system blade, reusable FDA UDI
- Device Name
- Retractors / Hooks EUDAMEDCaspar Blunt Retractor Blade 60mm x 23mm FDA UDI
- Model / Reference
- 749-1160-2 EUDAMEDFDA UDI
- Description
- Caspar Blunt Retractor Blade 60mm x 23mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- M930749116020 EUDAMEDFDA UDI
- Basic UDI-DI
- ++M930004PZ EUDAMED
- FDA Product Code
- GAD FDA UDI
- EMDN Code
- L110502 NERVES AND VESSELS HOOK RETRACTORS, REUSABLE EUDAMED
- GMDN Term
- Surgical retractor/retraction system blade, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Spain EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
Yes
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
No
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Category: Surgical retractor/retraction system blade, reusable
Life Instruments by Life Instrument Corporation — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Life Instrument Corporation
Sources (2)
- FDA UDI 39efeed8-f104-42cb-a1b5-4f6dfb57be2d 33 fields · synced Jun 18, 2026
- EUDAMED c48bf7d7-0e23-425d-b177-6b48552defc1 61 fields · synced Jun 18, 2026