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Insyte Autoguard 382924

by Becton, Dickinson and Company

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 26 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00382903829248 UDI-DI Date13 Feb 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 26 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Insyte Autoguard
Generic Name
Peripheral intravenous cannula
Model / Ref / Catalog
382924
Primary DI / UDI-DI
00382903829248
510(k) Number
FDA Product Code
DYB, FOZ
GMDN Term
Peripheral intravenous cannula
Device Class
Class II
Regulation Number
870.1340, 880.5200
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional
Size
Length — 32 Millimeter

Related devices

Cleared under the same submission (K251654)

Show all (12)

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No