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Bemis MCANISTER1

by Bemis Manufacturing Company

Bemis MCANISTER1 is a Class II device made by Bemis Manufacturing Company, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10073088153118), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10073088153118 UDI-DI Date24 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  • Withdrawn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

Trade name
Bemis
Generic name
Surgical suction system collection container, single-use
Model / Ref / Catalog
MCANISTER1
Primary DI / UDI-DI
10073088153118
FDA product code
KDQ
GMDN term
Surgical suction system collection container, single-use
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 800 Milliliter

Related devices

Category: Surgical suction system collection container, single-use

Similar devices in this category

Other devices filed under Surgical suction system collection container, single-use.

Other devices from Bemis Manufacturing Company

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Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)