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Cytal® WSR1635

by Acell, Inc.

Cytal® WSR1635 is a device classified as Unclassified made by Acell, Inc., listed in FDA GUDID since 16 Dec 2019 (UDI-DI 00386190001837), 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 Number00386190001837 UDI-DI Date16 Dec 2019ListedStatusListed 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  • Withdrawn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
Cytal®
Generic name
Animal-derived wound matrix dressing
Model / Ref / Catalog
WSR1635
Primary DI / UDI-DI
00386190001837
FDA product code
KGN
GMDN term
Animal-derived wound matrix dressing
Device class
U
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe
Size
Length — 35 Centimeter
Width — 16 Centimeter

Related devices

Category: Animal-derived wound matrix dressing

Similar devices

Other devices filed under FDA product code KGN (DRESSING, WOUND, COLLAGEN).

Other devices from Acell, Inc.

See all devices from Acell, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (9, all answered No)