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Sahara-III Maxitherm 115V

by Transmed Medizintechnik GmbH & Co. KG

Sahara-III Maxitherm 115V (97.8710.802) is a Class II device made by Transmed Medizintechnik GmbH & Co. KG, listed in FDA GUDID since 15 Aug 2016 (UDI-DI 04028339710939), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04028339710939 UDI-DI Date15 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Sahara
Generic name
Cryopreserved blood/tissue thawing unit
Model / Ref / Catalog
SAHARA-III MAXITHERM 115V, 97.8710.802
Primary DI / UDI-DI
04028339710939
FDA product code
KZL
GMDN term
Cryopreserved blood/tissue thawing unit
Device class
Class II
Regulation number
864.9205
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cryopreserved blood/tissue thawing unit

Similar devices in this category

Other devices filed under Cryopreserved blood/tissue thawing unit.

Other devices from Transmed Medizintechnik GmbH & Co. KG

Properties

  • Serial number
Other properties (14, all answered No)