Identity
- Trade Name
- MAMMOGRAM CAPE FDA UDI
- Generic Name
- Patient gown, reusable FDA UDI
- Device Name
- MAMMOGRAM CAPE KAUM ROSEBUD OSFA RM (98 8048) USE: 76S51380 FDA UDI
- Model / Reference
- 76SQ7880 FDA UDI
- Description
- MAMMOGRAM CAPE KAUM ROSEBUD OSFA RM (98 8048) USE: 76S51380 FDA UDI
Identifiers
- Catalog Number
- 76SQ7880 FDA UDI
- Primary DI / UDI-DI
- 00634916251975 FDA UDI
- FDA Product Code
- FME FDA UDI
- GMDN Term
- Patient gown, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6265 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Mammogram Cape by Standard Textile Co., 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 |
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Manufacturer
- Manufacturer
- Standard Textile Co., Inc.
Sources (1)
- FDA UDI 7f9f8da4-0110-4925-a870-4c873a39830b 36 fields · synced May 30, 2026