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Constellation®

FDA UDI

Class II (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
CONSTELLATION® FDA UDI
Generic Name
Closed-wound/centesis drainage receptacle FDA UDI
Device Name
Stand Alcone Drain Bags FDA UDI
Model / Reference
8065751162 FDA UDI
Description
Stand Alcone Drain Bags FDA UDI

Identifiers

Primary DI / UDI-DI
00380657511624 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Closed-wound/centesis drainage receptacle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 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

Category: Closed-wound/centesis drainage receptacle

Constellation® by Alcon Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound/centesis drainage receptacle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5d1dcf4d-2223-4d50-8d0f-1e226f55009e 34 fields · synced May 30, 2026