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Insight Instruments, Inc. Vitreous Biopsy Probe 27 Ga

FDA UDI

Class II (US FDA UDI)

by Insight Instruments, Inc.

Identity

Trade Name
Insight Instruments, Inc. Vitreous Biopsy Probe 27 Ga FDA UDI
Generic Name
Vitrectomy system handpiece tip FDA UDI
Device Name
1 Each Sterile Disposable 27 Ga Vitreous Biopsy Probe for use with the INTRECTOR® Kit FDA UDI
Model / Reference
71007.100 FDA UDI
Description
1 Each Sterile Disposable 27 Ga Vitreous Biopsy Probe for use with the INTRECTOR® Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00852475007004 FDA UDI
FDA Product Code
HKP FDA UDI
GMDN Term
Vitrectomy system handpiece tip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4150 FDA UDI
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

No

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 — 27 Gauge FDA UDI

Category: Vitrectomy system handpiece tip

Insight Instruments, Inc. Vitreous Biopsy Probe 27 Ga by Insight Instruments, Inc. — Class II — 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

Manufacturer
Insight Instruments, Inc.

Sources (1)

  • FDA UDI 48eb96b2-1e06-4208-9da8-7721ac4e69dd 36 fields · synced Jun 6, 2026