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Sahara

FDA UDI

Class II (US FDA UDI)

by Transmed Medizintechnik GmbH & Co. KG

Identity

Trade Name
SAHARA FDA UDI
Generic Name
Cryopreserved blood/tissue thawing unit FDA UDI
Device Name
Warming equipment with heatable agitation plate for thawing and warming of up to 3 blood components packed in plastic bags FDA UDI
Model / Reference
SAHARA-III basic model 115V FDA UDI
Description
Warming equipment with heatable agitation plate for thawing and warming of up to 3 blood components packed in plastic bags FDA UDI

Identifiers

Catalog Number
97.8710.502 FDA UDI
Primary DI / UDI-DI
04028339710236 FDA UDI
FDA Product Code
KZL FDA UDI
GMDN Term
Cryopreserved blood/tissue thawing unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9205 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: Cryopreserved blood/tissue thawing unit

Sahara by Transmed Medizintechnik GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cryopreserved blood/tissue thawing unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Transmed Medizintechnik GmbH & Co. KG

Sources (1)

  • FDA UDI 2c87bcb2-f4c9-44f8-89f9-3c61d5c9818b 34 fields · synced May 30, 2026