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SealSafe 760020P

by Andwin Scientific

SealSafe 760020P is a vial/bottle adaptor (FDA Class I; FDA product code IQG, Adaptor, Holder, Syringe) made by Andwin Scientific, listed in FDA GUDID since 14 Aug 2025 (UDI-DI 00187207000481), 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 Number00187207000481 UDI-DI Date14 Aug 2025ListedStatusListed 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  • Withdrawn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

Trade name
SealSafe
Generic name
Vial/bottle adaptor, non-hermetic
Model / reference
760020P
Primary DI / UDI-DI
00187207000481
FDA product code
IQG
GMDN term
Vial/bottle adaptor, non-hermetic
Device class
Class I
Regulation number
890.5050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vial/bottle adaptor, non-hermetic

Similar devices in this category

Other devices filed under Vial/bottle adaptor, non-hermetic.

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Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)