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PolyMem MAX

by Ferris Mfg. Corp. 7 variants

PolyMem MAX (5045) is a Class I device made by Ferris Mfg. Corp., listed in FDA GUDID since 31 Aug 2020 (UDI-DI 10735471050458), 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 Number10735471050458 UDI-DI Date31 Aug 2020ListedStatusListed 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  • Withdrawn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
PolyMem
Generic name
Wound-nonadherent dressing, absorbent, non-antimicrobial
Model / Ref / Catalog
MAX, 5045
Primary DI / UDI-DI
10735471050458
FDA product code
KMF
GMDN term
Wound-nonadherent dressing, absorbent, non-antimicrobial
Device class
Class I
Regulation number
880.5090
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Wound-nonadherent dressing, absorbent, non-antimicrobial

Similar devices

Other devices filed under FDA product code KMF (Bandage, Liquid).

Other devices from Ferris Mfg. Corp.

See all devices from Ferris Mfg. Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Over-the-counter
Other properties (11, all answered No)