Na Dt-C

by Panpac Medical Corporation

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04715309121474 UDI-DI	Date18 Aug 2016Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Vaginal dilator
Model / Reference: DT-C

Primary DI / UDI-DI: 04715309121474
FDA Product Code: HDX
GMDN Term: Vaginal dilator

Device Class: Class II
Regulation Number: 884.3900
GUDID distribution status: In Commercial Distribution

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Properties

Single Use
Prescription Use
Combination Product
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (8)

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