Identity
- Trade Name
- RETRECTOR® FDA UDI
- Generic Name
- Vitrectomy system handpiece tip FDA UDI
- Device Name
- 1 RETRECTOR® Probe Kit containing 1 Each Syringe 10ml & 1 Each Disposable 23 Ga Vitrectomy Probe with retractable tip FDA UDI
- Model / Reference
- 71005 FDA UDI
- Description
- 1 RETRECTOR® Probe Kit containing 1 Each Syringe 10ml & 1 Each Disposable 23 Ga Vitrectomy Probe with retractable tip FDA UDI
Identifiers
- Catalog Number
- 71005 FDA UDI
- Primary DI / UDI-DI
- 00856222004674 FDA UDI
- GMDN Term
- Vitrectomy system handpiece tip FDA UDI
Classification
- 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
Yes
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
Dimensions & Sizes
- Size
- Needle Gauge — 23 Gauge FDA UDI
Category: Vitrectomy system handpiece tip
Retrector® by Insight Instruments, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Insight Instruments, Inc.
Sources (1)
- FDA UDI 11f845a9-9f0d-4fe8-bd48-08f3866b10c5 36 fields · synced May 30, 2026