Identity
- Trade Name
- MOUTH PROP CHILD-BLACK FDA UDI
- Generic Name
- Mouth gag, non-adjustable FDA UDI
- Model / Reference
- 10-6052B FDA UDI
Identifiers
- Primary DI / UDI-DI
- D928106052B1 FDA UDI
- FDA Product Code
- KBN FDA UDI
- GMDN Term
- Mouth gag, non-adjustable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Mouth gag, non-adjustable
Mouth Prop Child-Black by W.H. Holden, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Mouth gag, non-adjustable.
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Disposable E-Prop Mouth Props Medium — PRACTICON, INC. · Class I
- Instrapac — ROBINSON HEALTHCARE LIMITED · Class I
- Plasdent — PLASDENT CORP. · Class I
- Plasdent — PLASDENT CORP. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Surgical Direct — SURGICAL DIRECT, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- W.H. Holden, Inc.
Sources (1)
- FDA UDI a1424f3c-4157-462b-8ec4-17ddc7014913 32 fields · synced Jun 1, 2026