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Intrector®

FDA UDI

by Insight Instruments, Inc.

Identity

Trade Name
INTRECTOR® FDA UDI
Generic Name
Vitrectomy system FDA UDI
Device Name
INTRECTOR® Portable Vitrectomy System including REF: 71102 Power Unit & REF: 71101 Handpiece FDA UDI
Model / Reference
71200 FDA UDI
Description
INTRECTOR® Portable Vitrectomy System including REF: 71102 Power Unit & REF: 71101 Handpiece FDA UDI

Identifiers

Catalog Number
71200 FDA UDI
Primary DI / UDI-DI
00856222004759 FDA UDI
GMDN Term
Vitrectomy system FDA UDI

Classification

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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vitrectomy system

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

Similar devices

Also classified as Vitrectomy system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Insight Instruments, Inc.

Sources (1)

  • FDA UDI 8e249dbe-4931-4103-b970-8a24367a74f3 35 fields · synced May 30, 2026