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SCANLAN® Forceps 4004-157

by Scanlan International Inc United States GUDID

Product code DWP

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00846159035926 UDI-DIDate13 Nov 2025ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 23 Oct 2026)

Specification

GUDID · synced 23 Oct 2026

Trade Name
SCANLAN® Forceps
Generic Name
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Model / Ref / Catalog
4004-157
Primary DI / UDI-DI
00846159035926
FDA Product Code
DWP
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Device Class
Class II
Regulation Number
870.4475
Commercial Distribution
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from Scanlan International Inc

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Properties & raw data

Show properties, registry sources and raw records
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
Other properties (11)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI ed0e50d7-8a70-4dc0-b2c2-40ebff61301e 35 fields · synced 23 Oct 2026