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Betife 1.0

by Guangdong SouthVo Medical Technology Co., Ltd 4 variants

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 Number16976349773923 UDI-DI Date9 May 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  • Withdrawn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
Betife
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial
Model / Reference
1.0
Primary DI / UDI-DI
16976349773923
FDA Product Code
NAD
GMDN Term
Wound-nonadherent dressing, absorbent, non-antimicrobial
Device Class
Class I
Regulation Number
878.4020
GUDID distribution status
In Commercial Distribution

Other devices from Guangdong SouthVo Medical Technology Co., Ltd

See all devices from Guangdong SouthVo Medical Technology Co., Ltd →

Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

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