← Back to catalogue

De-/Recapper 900 FLEX ID, 115V

FDA UDI

Class I (US FDA UDI)

by Sarstedt Aktiengesellschaft & Co.KG

Identity

Trade Name
De-/Recapper 900 FLEX ID, 115V FDA UDI
Generic Name
Laboratory container/microscope slide robotic transfer system IVD FDA UDI
Model / Reference
90.2060.045 FDA UDI

Identifiers

Catalog Number
90.2060.045 FDA UDI
Primary DI / UDI-DI
04038917418539 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

De-/Recapper 900 FLEX ID, 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

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

Manufacturer

Manufacturer
Sarstedt Aktiengesellschaft & Co.KG

Sources (1)

  • FDA UDI f461baff-512c-49e5-840b-4495c9d777c5 34 fields · synced May 30, 2026