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Nella Next Reusable Vaginal Speculum NNM010

by Ceek Women's Health

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20860000270421 UDI-DI Date25 Jun 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Nella Next Reusable Vaginal Speculum
Generic Name
Vaginal speculum, reusable
Model / Reference
NNM010
Primary DI / UDI-DI
20860000270421
FDA Product Code
HIB
GMDN Term
Vaginal speculum, reusable
Device Class
Class II
Regulation Number
884.4530
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

From the manufacturer

Manufacturer's product page: Nella NEXT Reusable Vaginal Speculum

Other devices from Ceek Women's Health

See all devices from Ceek Women's Health →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No