Identity
- Trade Name
- DEPRESSOR FDA UDI
- Generic Name
- Orbital depressor, single-use FDA UDI
- Device Name
- SCHOCKERT DOUBLE-END SCLERAL DEPRESSOR SATIN 5-1/2 FDA UDI
- Model / Reference
- SCLERAL DEPRESSOR FDA UDI
- Description
- SCHOCKERT DOUBLE-END SCLERAL DEPRESSOR SATIN 5-1/2 FDA UDI
Identifiers
- Catalog Number
- SD500 FDA UDI
- Primary DI / UDI-DI
- B974SD5000 FDA UDI
- FDA Product Code
- HNX FDA UDI
- GMDN Term
- Orbital depressor, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Length — 5.5 Inch FDA UDI
Category: Orbital depressor, single-use
Depressor by Dr.frigz International(pvt)ltd, — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Dr.frigz International(pvt)ltd,
Sources (1)
- FDA UDI 4a5429df-ce89-4abe-a561-a257968a9b73 35 fields · synced Jun 8, 2026