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Ispan

FDA UDI

Class III (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
ISPAN FDA UDI
Generic Name
Vitreous/aqueous humour replacement medium, intraoperative FDA UDI
Device Name
ISPAN SF6 CONSTELLATION 125GM FDA UDI
Model / Reference
8065797005 FDA UDI
Description
ISPAN SF6 CONSTELLATION 125GM FDA UDI

Identifiers

Primary DI / UDI-DI
00380657970056 FDA UDI
FDA Product Code
LPO FDA UDI
GMDN Term
Vitreous/aqueous humour replacement medium, intraoperative FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
886.4270 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Dimensions & Sizes

Size
Weight — 125 Gram FDA UDI

Category: Vitreous/aqueous humour replacement medium, intraoperative

Ispan by Alcon Laboratories, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vitreous/aqueous humour replacement medium, intraoperative.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI da3f1c0d-b581-4cc1-91ac-95b06bdc2a5e 35 fields · synced May 30, 2026