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BVI Medical

FDA UDI

Class III (US FDA UDI)

by Airgas Therapeutics

Identity

Trade Name
BVI Medical FDA UDI
Generic Name
Vitreous/aqueous humour replacement medium, intraoperative FDA UDI
Device Name
ISPAN Gas, Perfluoropropane (C3F8); Cylinder: LD2; Valve: CGA 180; Retinal tamponade for use in pneumatic retinopexy. FDA UDI
Model / Reference
ISPAN FDA UDI
Description
ISPAN Gas, Perfluoropropane (C3F8); Cylinder: LD2; Valve: CGA 180; Retinal tamponade for use in pneumatic retinopexy. FDA UDI

Identifiers

Catalog Number
3R MDGLD2CB58 FDA UDI
Primary DI / UDI-DI
00819601025707 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

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

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
Weight — 125 Gram FDA UDI

Category: Vitreous/aqueous humour replacement medium, intraoperative

BVI Medical by Airgas Therapeutics — 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

Manufacturer
Airgas Therapeutics

Sources (1)

  • FDA UDI d10ae65c-40d0-475d-b27f-f0927a1c1b83 36 fields · synced May 30, 2026