Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Mouth gag, adjustable, reusable FDA UDI
- Device Name
- V. Mueller DAVIS-CROWE MOUTH GAG TONGUE DEPRESSOR BLADES NO 2-1/2 7.5 X 2.4CM WIDE FDA UDI
- Model / Reference
- MO161-001 FDA UDI
- Description
- V. Mueller DAVIS-CROWE MOUTH GAG TONGUE DEPRESSOR BLADES NO 2-1/2 7.5 X 2.4CM WIDE FDA UDI
Identifiers
- Catalog Number
- MO161-001 FDA UDI
- Primary DI / UDI-DI
- 10885403188244 FDA UDI
- FDA Product Code
- KBN FDA UDI
- GMDN Term
- Mouth gag, adjustable, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
V. Mueller by Carefusion 2200, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI 49db7e71-e145-4ef1-9297-81679973603a 36 fields · synced Sep 18, 2026