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Jaeger

FDA UDI

Class II (US FDA UDI)

by Jaeger Medical GmbH

Identity

Trade Name
Jaeger FDA UDI
Generic Name
Tissue embedding unit IVD FDA UDI
Device Name
Vyntus CART Basic FDA UDI
Model / Reference
V-859142-13 FDA UDI
Description
Vyntus CART Basic FDA UDI

Identifiers

Catalog Number
V-859142-13 FDA UDI
Primary DI / UDI-DI
34250892908213 FDA UDI
510(k) Number
K071753 FDA UDI
FDA Product Code
BTY FDA UDI
GMDN Term
Tissue embedding unit IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1890 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

Yes

FDA UDI

Category: Tissue embedding unit IVD

Jaeger by Jaeger Medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue embedding unit IVD.

Cleared under the same submission

K071753 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Jaeger Medical GmbH

Sources (1)

  • FDA UDI 0b1b232d-a8e3-4e71-99c4-ac585a18643c 37 fields · synced Jun 6, 2026