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Accel®

FDA UDI

Class II (US FDA UDI)

by B. Braun Melsungen Aktiengesellschaft

Identity

Trade Name
ACCEL® FDA UDI
Generic Name
Closed-wound drainage kit FDA UDI
Device Name
1000ML DRAINAGE BOTTLE, PVC-FREE FDA UDI
Model / Reference
622275 FDA UDI
Description
1000ML DRAINAGE BOTTLE, PVC-FREE FDA UDI

Identifiers

Catalog Number
622275 FDA UDI
Primary DI / UDI-DI
04046964613371 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Closed-wound drainage kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

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 — 1000.0 Milliliter FDA UDI

Category: Closed-wound drainage kit

Accel® by B. Braun Melsungen Aktiengesellschaft — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound drainage kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6d83ed9a-1b7a-4256-a7f0-58b88cf7f8f5 36 fields · synced May 29, 2026