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Atellica Direct Load

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica Direct Load FDA UDI
Generic Name
Specimen processing instrument IVD FDA UDI
Device Name
Atellica DL MODULE FDA UDI
Model / Reference
11068008 FDA UDI
Description
Atellica DL MODULE FDA UDI

Identifiers

Catalog Number
11068008 FDA UDI
Primary DI / UDI-DI
00630414002347 FDA UDI
510(k) Number
K151767 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Specimen processing instrument IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Specimen processing instrument IVD

Atellica Direct Load by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Specimen processing instrument IVD.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a93bd22b-7357-4431-8898-9e7741c8e024 36 fields · synced May 30, 2026