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Asept®

FDA UDI

Class I (US FDA UDI)

by B Braun Interventional Systems, Inc

Identity

Trade Name
ASEPT® FDA UDI
Generic Name
Wound drainage bag FDA UDI
Device Name
2,000 ML DRAINAGE BAG W PROCEDURE PACK FDA UDI
Model / Reference
622281 FDA UDI
Description
2,000 ML DRAINAGE BAG W PROCEDURE PACK FDA UDI

Identifiers

Catalog Number
622281 FDA UDI
Primary DI / UDI-DI
04046964317293 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
Wound drainage bag FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

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
Total Volume — 2000.0 Milliliter FDA UDI

Category: Wound drainage bag

Asept® by B Braun Interventional Systems, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound drainage bag.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B Braun Interventional Systems, Inc

Sources (1)

  • FDA UDI 004dda29-a202-48b0-aceb-8d9ae42999b2 37 fields · synced May 30, 2026