Identity
- Trade Name
- Medline FDA UDI
- Generic Name
- Medical equipment/instrument drape, reusable FDA UDI
- Device Name
- WRAPPER,INSTRMNT,STB,MG W/14 SLOTS&T FDA UDI
- Model / Reference
- MDTZ1024986AX FDA UDI
- Description
- WRAPPER,INSTRMNT,STB,MG W/14 SLOTS&T FDA UDI
Identifiers
- Catalog Number
- MDTZ1024986AX FDA UDI
- Primary DI / UDI-DI
- 10888277419261 FDA UDI
- FDA Product Code
- FRG FDA UDI
- GMDN Term
- Medical equipment/instrument drape, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6850 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
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
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
Category: Medical equipment/instrument drape, reusable
Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Medline Industries, Inc.
Sources (1)
- FDA UDI d6ab1ac8-94f6-447f-86a5-01c0892e5b4b 35 fields · synced May 31, 2026