← Back to catalogue

Diacap®

FDA UDI

Class II (US FDA UDI)

by B.Braun Avitum AG

Identity

Trade Name
Diacap® FDA UDI
Generic Name
Hollow-fibre haemodialysis dialyser, single-use FDA UDI
Device Name
Diacap® Pro 13H FDA UDI
Model / Reference
720DH13 FDA UDI
Description
Diacap® Pro 13H FDA UDI

Identifiers

Catalog Number
720DH13 FDA UDI
Primary DI / UDI-DI
04046964610776 FDA UDI
FDA Product Code
KDI FDA UDI
GMDN Term
Hollow-fibre haemodialysis dialyser, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5860 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

No

FDA UDI

Category: Hollow-fibre haemodialysis dialyser, single-use

Diacap® by B.Braun Avitum AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hollow-fibre haemodialysis dialyser, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
B.Braun Avitum AG

Sources (1)

  • FDA UDI 40377a0b-1d79-4ecd-b6a6-b8ce8104bbe7 37 fields · synced May 30, 2026