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VitalTemp™ Universal Pad, 2PK, US

by ZOLL Circulation, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10849111076293 UDI-DI Date12 Dec 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
VitalTemp™
Generic Name
External circulating-fluid core temperature regulation system pad, single-use
Model / Ref / Catalog
VitalTemp™ Universal Pad, 2PK, US, 8700-001131
Primary DI / UDI-DI
10849111076293
FDA Product Code
NZE
GMDN Term
External circulating-fluid core temperature regulation system pad, single-use
Device Class
Class II
Regulation Number
870.5900
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Other devices from ZOLL Circulation, Inc.

See all devices from ZOLL Circulation, Inc. →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No