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Solventum™ Tegaderm™ 1877-2100

by Solventum US LLC

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 Number00197998001246 UDI-DI Date23 Aug 2026ListedStatusListed 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  • Withdrawn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
Solventum™ Tegaderm™
Generic Name
Wearable percutaneous catheter/tube holder, single-use
Model / Ref / Catalog
1877-2100
Description
Solventum™ PICC/CVC Securement Device + Tegaderm™ CHG I.V. Securement Dressing, 1877-2100, 3-1/2 in x 4-1/2 in, 20/CAR, 4 CAR/CS
Primary DI / UDI-DI
00197998001246
FDA Product Code
PEZ
GMDN Term
Wearable percutaneous catheter/tube holder, single-use
Device Class
Class II
Regulation Number
880.5200
GUDID distribution status
In Commercial Distribution

Other devices from Solventum US LLC

See all devices from Solventum US LLC →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Combination Product
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (6)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No