McKesson 100199
by Mckesson Medical-Surgical Inc.
McKesson 100199 is a Class I device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 26 Jul 2021 (UDI-DI 00612479194816), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00612479194816 | Date26 Jul 2021 | StatusListed |
Official records
- AccessGUDID record 00612479194816
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- McKesson
- Generic name
- Cast construction material
- Model / reference
- 100199
- Primary DI / UDI-DI
- 00612479194816
- FDA product code
- ITG
- GMDN term
- Cast construction material
- Device class
- Class I
- Regulation number
- 890.3025
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code ITG (Bandage, Cast).
- HEXCELITE by Hexcel Medical
- URETHANE ORTHOPAEDIC CASTING TAPE by Hexcel Medical
- Webril 3175 3175- by Cardinal Health 200, LLC
- Webril 2059 2059- by Cardinal Health 200, LLC
- DELTA-LITE by Johnson & Johnson Professionals, Inc.
- ORTHOPEDIC CASTING TAPE MAXCAST by Cutter Laboratories, Inc.
- CONFORMA(TM) PLASTER BANDAGES by The Kendal Co.
- NON WETTING UNDERCAST PADDING by American Medical Disposable, Inc.
- TAPE, LIGHTCAST II WB by Solar Laboratories, Inc.
- CELLONA by Secol Co.