Identity
- Trade Name
- Life Instruments FDA UDI
- Generic Name
- Hand-held surgical retractor, reusable FDA UDI
- Device Name
- Cobra Retractor Thin Tip Ball Handle FDA UDI
- Model / Reference
- 742-1215-0-2 FDA UDI
- Description
- Cobra Retractor Thin Tip Ball Handle FDA UDI
Identifiers
- Primary DI / UDI-DI
- M9307421215020 FDA UDI
- FDA Product Code
- GAD FDA UDI
- GMDN Term
- Hand-held surgical retractor, reusable 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Hand-held surgical retractor, reusable
A comprehensive 2-3 paragraph SEO description for Life Instruments Cobra Retractor Thin Tip Ball Handle, a reliable hand-held surgical retractor designed to provide precise control during open surgery. This device is intended for general plastic surgery procedures and is not dedicated to ophthalmic or small nerve/vessel retraction.
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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
- Life Instrument Corporation
Sources (1)
- FDA UDI 5da99f4f-8cb6-488e-9e1d-335c715f20a0 33 fields · synced Jul 19, 2026