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Intrector®

FDA UDI

by Insight Instruments, Inc.

Identity

Trade Name
INTRECTOR® FDA UDI
Generic Name
Vitrectomy system handpiece tip FDA UDI
Device Name
1 INTRECTOR® Probe Kit containing 1 Each Syringe 1ml, 1 Each Syringe 3ml, & 1 Each Disposable 23 Ga Vitrectomy Probe FDA UDI
Model / Reference
71004 FDA UDI
Description
1 INTRECTOR® Probe Kit containing 1 Each Syringe 1ml, 1 Each Syringe 3ml, & 1 Each Disposable 23 Ga Vitrectomy Probe FDA UDI

Identifiers

Catalog Number
71004 FDA UDI
Primary DI / UDI-DI
00856222004636 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

Intrector® by Insight Instruments, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vitrectomy system handpiece tip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 29218976-7f55-4fd5-b76e-8e0101ce61df 36 fields · synced May 30, 2026