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Recapper RC1200 LiaisonXL, 115V

FDA UDI

Class I (US FDA UDI)

by Sarstedt Aktiengesellschaft & Co.KG

Identity

Trade Name
Recapper RC1200 LiaisonXL,115V FDA UDI
Generic Name
Laboratory container/microscope slide robotic transfer system IVD FDA UDI
Model / Reference
90.197.018 FDA UDI

Identifiers

Catalog Number
90.197.018 FDA UDI
Primary DI / UDI-DI
04038917426879 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Laboratory container/microscope slide robotic transfer system IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laboratory container/microscope slide robotic transfer system IVD

Recapper RC1200 LiaisonXL, 115V by Sarstedt Aktiengesellschaft & Co.KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory container/microscope slide robotic transfer system IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d3f9b4f-1557-4578-9be2-b6add2666794 34 fields · synced May 30, 2026