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Dt-B/M

by Panpac Medical Corporation

Dt-B/M is a Class II device made by Panpac Medical Corporation, listed in FDA GUDID since 10 Sep 2016 (UDI-DI 04715309122181), 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 Number04715309122181 UDI-DI Date10 Sep 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  • Withdrawn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

Generic name
Vaginal dilator
Model / reference
DT-B/M
Primary DI / UDI-DI
04715309122181
FDA product code
HDX
GMDN term
Vaginal dilator
Device class
Class II
Regulation number
884.3900
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vaginal dilator

Other devices from Panpac Medical Corporation

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    Class II

  • SH4-W

    Class II

  • D6-W

    Class II

  • CUd0-W

    Class II

See all devices from Panpac Medical Corporation →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)