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Exmoor Mk/72/A/N/E106

by Exmoor Plastics Limited

Exmoor Mk/72/A/N/E106 (MK72ANE106) is a Class I device made by Exmoor Plastics Limited, listed in FDA GUDID since 8 Oct 2018 (UDI-DI 05060180254513), registry data as of 12 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060180254513 UDI-DI Date8 Oct 2018ListedStatusListed 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  • Withdrawn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
Exmoor
Generic name
Secretion suction kit
Model / Ref / Catalog
MK/72/A/N/E106, MK72ANE106
Primary DI / UDI-DI
05060180254513
FDA product code
JYP
GMDN term
Secretion suction kit
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution

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Properties

  • Supplied sterile
  • Single use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)