Identity
- Trade Name
- HALYARD FDA UDI
- Generic Name
- Patient surgical drape, single-use FDA UDI
- Device Name
- BASICS* Obstetrics Drapes_38 x 60 in._Sterile_7EA/CS FDA UDI
- Model / Reference
- 49900 FDA UDI
- Description
- BASICS* Obstetrics Drapes_38 x 60 in._Sterile_7EA/CS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 16931918117218 FDA UDI
- FDA Product Code
- PUI FDA UDI
- GMDN Term
- Patient surgical drape, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4370 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Patient surgical drape, single-use
Halyard by GRI Medical & Electronic Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Patient surgical drape, single-use.
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- Halyard — O&M HALYARD, INC. · Class II
- MICROTEK — Microtek Medical LLC · Class II
- MICROTEK — Microtek Medical LLC · Class II
- PREFERRED MEDICAL PRODUCTS, LLC — PREFERRED MEDICAL PRODUCTS, LLC · Class II
- Halyard — O&M HALYARD, INC. · Class II
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
- GRI Medical & Electronic Technology Co., Ltd.
Sources (1)
- FDA UDI c4d424b3-cbdf-406b-a292-19352eb38bc5 34 fields · synced Sep 18, 2026